Discussion:
Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from UCSC Genome Browser
Edge Edge
2012-06-26 15:41:19 UTC
Permalink
Dear Professor,
Can I know that how to extract the information (such as chromosome number,  position start and position ) of human hg19 3'-UTR,  5'-UTR, rRNA, tRNA from UCSC Genome Browser?

I got extract rRNA and tRNA by using the following method:
* Select "All Tables" from the group drop-down list
* Select the "rmsk" table from the table drop-down list
* Choose "GTF" as the output format / Choose "Sequence" as the output format
* Type a filename in "output file" so your browser downloads the result
* Click "create" next to filter
* Next to "repClass," type rRNA
* Next to free-form query, select "OR" and type repClass = "tRNA"
* Click submit on that page, then get output on the main page

However, when I check the position of rRNA and tRNA in GTF format and Sequence format.
It shown difference nucleotide.
Can I know how to solve this issue?
I just wanna to make sure the position of rRNA and tRNA in GTF format is tally with the position and chromosome shown in Sequence format.
Can I know how to get all the info regarding human hg19 3'-UTR,  5'-UTR, rRNA, tRNA from UCSC Genome Browser?

Many thanks for any advice.

best regards
Edge
Research Student 
Steve Heitner
2012-06-26 18:16:59 UTC
Permalink
Hello, Edge.

I repeated the steps you provided and I did not encounter a discrepancy
between the coordinates of the two queries. I would also like to add that
you do not need to set "group" to "All Tables" in order to use the rmsk
table. You can set "group" to "Variation and Repeats" and set "track" to
"RepeatMasker".

If you would like the coordinates of 5' UTR and 3' UTR regions, you will
need to use a gene track like UCSC Genes or RefSeq Genes. You can do so by
performing the following steps:

1. Set the following options:
Group: Genes and Gene Prediction Tracks
Track: UCSC Genes
Table: knownGene
Output format: sequence

2. Click the "get output" button

3. Select "genomic" and click the "submit" button

4. Check the "5' UTR Exons" and "3' UTR Exons" checkboxes and select any
other options you desire

5. Click the "get sequence" button

Note that the output here will not distinguish 5' UTR sequences from 3' UTR
sequences. If you want to distinguish 5' UTR sequences from 3' UTR
sequences, you will want to make two separate queries.

Please contact us again at ***@soe.ucsc.edu if you have any further
questions.

---
Steve Heitner
UCSC Genome Bioinformatics Group

-----Original Message-----
From: genome-***@soe.ucsc.edu [mailto:genome-***@soe.ucsc.edu] On
Behalf Of Edge Edge
Sent: Tuesday, June 26, 2012 8:41 AM
To: ***@soe.ucsc.edu
Cc: genome-***@soe.ucsc.edu
Subject: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from UCSC
Genome Browser

Dear Professor,
Can I know that how to extract the information (such as chromosome number,
 position start and position ) of human hg19 3'-UTR,  5'-UTR, rRNA, tRNA
from UCSC Genome Browser?

I got extract rRNA and tRNA by using the following method:
* Select "All Tables" from the group drop-down list
* Select the "rmsk" table from the table drop-down list
* Choose "GTF" as the output format / Choose "Sequence" as the
output format
* Type a filename in "output file" so your browser downloads the
result
* Click "create" next to filter
* Next to "repClass," type rRNA
* Next to free-form query, select "OR" and type repClass = "tRNA"
* Click submit on that page, then get output on the main page

However, when I check the position of rRNA and tRNA in GTF format and
Sequence format.
It shown difference nucleotide.
Can I know how to solve this issue?
I just wanna to make sure the position of rRNA and tRNA in GTF format is
tally with the position and chromosome shown in Sequence format.
Can I know how to get all the info regarding human hg19 3'-UTR,  5'-UTR,
rRNA, tRNA from UCSC Genome Browser?

Many thanks for any advice.

best regards
Edge
Research Student 
_______________________________________________
Genome maillist - ***@soe.ucsc.edu
https://lists.soe.ucsc.edu/mailman/listinfo/genome
Edge Edge
2012-06-27 01:32:54 UTC
Permalink
Dear Professor,

Many thanks for your advice.
I able to get all the rRNA, tRNA, 3'-UTR and 5'-UTR right now.

Below is one of the rRNA, RN45S which I able to find in NCBI, http://www.ncbi.nlm.nih.gov/nucleotide/374429547?report=genbank&log$=nuclalign&blast_rank=1&RID=YMRWVVSN01N
From the NCBI link, it shown that RN45S is located at chromosome 22.
However, I fail to get its info from UCSC :(

Do you have any idea regarding it?

Apart from that, can I know what is the difference between UCSC gene and Refseq Gene?
For me, both are exactly the same?

Thanks again and looking forward to hear from you :)

best regards
Edge
Research Student



________________________________
From: Steve Heitner <***@soe.ucsc.edu>
To: 'Edge Edge' <***@yahoo.com>; ***@soe.ucsc.edu
Sent: Wednesday, June 27, 2012 2:16 AM
Subject: RE: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from UCSC Genome Browser

Hello, Edge.

I repeated the steps you provided and I did not encounter a discrepancy
between the coordinates of the two queries.  I would also like to add that
you do not need to set "group" to "All Tables" in order to use the rmsk
table.  You can set "group" to "Variation and Repeats" and set "track" to
"RepeatMasker".

If you would like the coordinates of 5' UTR and 3' UTR regions, you will
need to use a gene track like UCSC Genes or RefSeq Genes.  You can do so by
performing the following steps:

1. Set the following options:
Group: Genes and Gene Prediction Tracks
Track: UCSC Genes
Table: knownGene
Output format: sequence

2. Click the "get output" button

3. Select "genomic" and click the "submit" button

4. Check the "5' UTR Exons" and "3' UTR Exons" checkboxes and select any
other options you desire

5. Click the "get sequence" button

Note that the output here will not distinguish 5' UTR sequences from 3' UTR
sequences.  If you want to distinguish 5' UTR sequences from 3' UTR
sequences, you will want to make two separate queries.

Please contact us again at ***@soe.ucsc.edu if you have any further
questions.

---
Steve Heitner
UCSC Genome Bioinformatics Group

-----Original Message-----
From: genome-***@soe.ucsc.edu [mailto:genome-***@soe.ucsc.edu] On
Behalf Of Edge Edge
Sent: Tuesday, June 26, 2012 8:41 AM
To: ***@soe.ucsc.edu
Cc: genome-***@soe.ucsc.edu
Subject: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from UCSC
Genome Browser

Dear Professor,
Can I know that how to extract the information (such as chromosome number,
 position start and position ) of human hg19 3'-UTR,  5'-UTR, rRNA, tRNA
from UCSC Genome Browser?

I got extract rRNA and tRNA by using the following method:
    * Select "All Tables" from the group drop-down list
    * Select the "rmsk" table from the table drop-down list
    * Choose "GTF" as the output format / Choose "Sequence" as the
output format
    * Type a filename in "output file" so your browser downloads the
result
    * Click "create" next to filter
    * Next to "repClass," type rRNA
    * Next to free-form query, select "OR" and type repClass = "tRNA"
    * Click submit on that page, then get output on the main page

However, when I check the position of rRNA and tRNA in GTF format and
Sequence format.
It shown difference nucleotide.
Can I know how to solve this issue?
I just wanna to make sure the position of rRNA and tRNA in GTF format is
tally with the position and chromosome shown in Sequence format.
Can I know how to get all the info regarding human hg19 3'-UTR,  5'-UTR,
rRNA, tRNA from UCSC Genome Browser?

Many thanks for any advice.

best regards
Edge
Research Student 
_______________________________________________
Genome maillist  -  ***@soe.ucsc.edu
https://lists.soe.ucsc.edu/mailman/listinfo/genome
Edge Edge
2012-06-27 03:36:52 UTC
Permalink
Dear Professor,
hg19_knownGene_uc010nxq.1 range=chr1:11874-12189 5'pad=0 3'pad=0 strand=+ repeatMasking=none
CTTGCCGTCAGCCTTTTCTTTGACCTCTTCTTTCTGTTCATGTGTATTTG
CTGTCTCTTAGCCCAGACTTCCCGTGTCCTTTCCACCGGGCCTTTGAGAG
GTCACAGGGTCTTGATGCTGTGGTCTTCATCTGCAGGTGTCTGACTTCCA
GCAACTGCTGGCCTGTGCCAGGGTGCAAGCTGAGCACTGGAGTGGAGTTT
TCCTGTGGAGAGGAGCCATGCCTAGAGTGGGATGGGCCATTGTTCATCTT
CTGGCCCCTGTTGTCTGCATGTAACTTAATACCACAACCAGGCATAGGGG
AAAGATTGGAGGAAAG
hg19_knownGene_uc001aaa.3 range=chr1:11874-14409 5'pad=0 3'pad=0 strand=+ repeatMasking=none
CTTGCCGTCAGCCTTTTCTTTGACCTCTTCTTTCTGTTCATGTGTATTTG
CTGTCTCTTAGCCCAGACTTCCCGTGTCCTTTCCACCGGGCCTTTGAGAG
GTCACAGGGTCTTGATGCTGTGGTCTTCATCTGCAGGTGTCTGACTTCCA
GCAACTGCTGGCCTGTGCCAGGGTGCAAGCTGAGCACTGGAGTGGAGTTT
TCCTGTGGAGAGGAGCCATGCCTAGAGTGGGATGGGCCATTGTTCATCTT
CTGGCCCCTGTTGTCTGCATGTAACTTAATACCACAACCAGGCATAGGGG
AAAGATTGGAGGAAAGATGAGTGAGAGCATCAACTTCTCTCACAACCTAG
GCCAGTGTGTGGTGATGCCAGGCATGCCCTTCCCCAGCATCAGGTCTCCA
GAGCTGCAGAAGACGACGGCCGACTTGGATCACACTCTTGTGAGTGTCCC
CAGTGTTGCAGAGGCAGGGCCATCAGGCACCAAAGGGATTCTGCCAGCAT
AGTGCTCCTGGACCAGTGATACACCCGGCACCCTGTCCTGGACACGCTGT
TGGCCTGGATCTGAGCCCTGGTGGAGGTCAAAGCCACCTTTGGTTCTGCC
ATTGCTGCTGTGTGGAAGTTCACTCCTGCCTTTTCCTTTCCCTAGAGCCT
CCACCACCCCGAGATCACATTTCTCACTGCCTTTTGTCTGCCCAGTTTCA
CCAGAAGTAGGCCTCTTCCTGACAGGCAGCTGCACCACTGCCTGGCGCTG
TGCCCTTCCTTTGCTCTGCCCGCTGGAGACGGTGTTTGTCATGGGCCTGG
TCTGCAGGGATCCTGCTACAAAGGTGAAACCCAGGAGAGTGTGGAGTCCA
GAGTGTTGCCAGGACCCAGGCACAGGCATTAGTGCCCGTTGGAGAAAACA
GGGGAATCCCGAAGAAATGGTGGGTCCTGGCCATCCGTGAGATCTTCCCA
GGGCAGCTCCCCTCTGTGGAATCCAATCTGTCTTCCATCCTGCGTGGCCG
AGGGCCAGGCTTCTCACTGGGCCTCTGCAGGAGGCTGCCATTTGTCCTGC
CCACCTTCTTAGAAGCGAGACGGAGCAGACCCATCTGCTACTGCCCTTTC
TATAATAACTAAAGTTAGCTGCCCTGGACTATTCACCCCCTAGTCTCAAT
TTAAGAAGATCCCCATGGCCACAGGGCCCCTGCCTGGGGGCTTGTCACCT
CCCCCACCTTCTTCCTGAGTCATTCCTGCAGCCTTGCTCCCTAACCTGCC
CCACAGCCTTGCCTGGATTTCTATCTCCCTGGCTTGGTGCCAGTTCCTCC
AAGTCGATGGCACCTCCCTCCCTCTCAACCACTTGAGCAAACTCCAAGAC
ATCTTCTACCCCAACACCAGCAATTGTGCCAAGGGCCATTAGGCTCTCAG
CATGACTATTTTTAGAGACCCCGTGTCTGTCACTGAAACCTTTTTTGTGG
GAGACTATTCCTCCCATCTGCAACAGCTGCCCCTGCTGACTGCCCTTCTC
TCCTCCCTCTCATCCCAGAGAAACAGGTCAGCTGGGAGCTTCTGCCCCCA
CTGCCTAGGGACCAACAGGGGCAGGAGGCAGTCACTGACCCCGAGACGTT
TGCATCCTGCACAGCTAGAGATCCTTTATTAAAAGCACACTGTTGGTTTC
TG
My problem is that how come 3'-UTR and 5'-UTR can be at the same region in human genome?
Do you have any distinguish which part is the 3'-UTR and 5'-UTR?
Based on my understanding, the human genome structure should be promoter-5'-UTR-exon-intron-3'UTR-terminator
Thus I confused that the region of 3'-UTR and 5'-UTR is fall within the same region.

Many thanks for advice to solve my doubts.

best regards
Edge
Research Student



________________________________
From: Steve Heitner <***@soe.ucsc.edu>
To: 'Edge Edge' <***@yahoo.com>; ***@soe.ucsc.edu
Sent: Wednesday, June 27, 2012 2:16 AM
Subject: RE: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from UCSC Genome Browser

Hello, Edge.

I repeated the steps you provided and I did not encounter a discrepancy
between the coordinates of the two queries.  I would also like to add that
you do not need to set "group" to "All Tables" in order to use the rmsk
table.  You can set "group" to "Variation and Repeats" and set "track" to
"RepeatMasker".

If you would like the coordinates of 5' UTR and 3' UTR regions, you will
need to use a gene track like UCSC Genes or RefSeq Genes.  You can do so by
performing the following steps:

1. Set the following options:
Group: Genes and Gene Prediction Tracks
Track: UCSC Genes
Table: knownGene
Output format: sequence

2. Click the "get output" button

3. Select "genomic" and click the "submit" button

4. Check the "5' UTR Exons" and "3' UTR Exons" checkboxes and select any
other options you desire

5. Click the "get sequence" button

Note that the output here will not distinguish 5' UTR sequences from 3' UTR
sequences.  If you want to distinguish 5' UTR sequences from 3' UTR
sequences, you will want to make two separate queries.

Please contact us again at ***@soe.ucsc.edu if you have any further
questions.

---
Steve Heitner
UCSC Genome Bioinformatics Group

-----Original Message-----
From: genome-***@soe.ucsc.edu [mailto:genome-***@soe.ucsc.edu] On
Behalf Of Edge Edge
Sent: Tuesday, June 26, 2012 8:41 AM
To: ***@soe.ucsc.edu
Cc: genome-***@soe.ucsc.edu
Subject: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from UCSC
Genome Browser

Dear Professor,
Can I know that how to extract the information (such as chromosome number,
 position start and position ) of human hg19 3'-UTR,  5'-UTR, rRNA, tRNA
from UCSC Genome Browser?

I got extract rRNA and tRNA by using the following method:
    * Select "All Tables" from the group drop-down list
    * Select the "rmsk" table from the table drop-down list
    * Choose "GTF" as the output format / Choose "Sequence" as the
output format
    * Type a filename in "output file" so your browser downloads the
result
    * Click "create" next to filter
    * Next to "repClass," type rRNA
    * Next to free-form query, select "OR" and type repClass = "tRNA"
    * Click submit on that page, then get output on the main page

However, when I check the position of rRNA and tRNA in GTF format and
Sequence format.
It shown difference nucleotide.
Can I know how to solve this issue?
I just wanna to make sure the position of rRNA and tRNA in GTF format is
tally with the position and chromosome shown in Sequence format.
Can I know how to get all the info regarding human hg19 3'-UTR,  5'-UTR,
rRNA, tRNA from UCSC Genome Browser?

Many thanks for any advice.

best regards
Edge
Research Student 
_______________________________________________
Genome maillist  -  ***@soe.ucsc.edu
https://lists.soe.ucsc.edu/mailman/listinfo/genome
Steve Heitner
2012-06-27 19:24:07 UTC
Permalink
Hello, Edge.



The UCSC Genes track is produced by UCSC while the RefSeq Genes track comes
from NCBI. Many of the items from these tracks correspond with each other,
but the RefSeq Genes track is updated nightly while the UCSC Genes track is
updated less often, so you will find that some of the newer items in the
RefSeq Genes track will not be present in the UCSC Genes track. This is
almost certainly the case with NR_046235 as the Genbank page at
http://www.ncbi.nlm.nih.gov/nucleotide/374429547?report=genbank reports that
this is the first revision and it was released on 13-May-2012. To find the
date that a track was last updated, go to that track's description page by
clicking the vertical gray bar at the left side of the Browser's graphical
display or by clicking the track name in the track listing below the
graphical display. You will see "Data last updated" near the top of the
page.



For your question regarding uc001aaa.3 and uc010nxr.1 from the UCSC Genes
track, if you browse to h19 coordinates chr1:11,874-14,409, you will see
that these are both transcript variants of the same gene, DDX11L1
(http://www.ncbi.nlm.nih.gov/nuccore/NR_046018?report=GenBank).



Similar to the above question, the 5' UTR and 3' UTR sequences you refer to
belong to different transcript variants. If you again browse to hg19
chr1:11,874-14,409 here, you will see that uc010nxq.1 has only one 5' UTR on
exon 1 and only one 3' UTR on exon 3. With uc001aaa.3, the entire region is
untranslated and thus the entire transcript is considered 3' UTR. This is
why you see overlap between the 5' UTR of uc010nxq.1 and the 3' UTR of
uc001aaa.3 and this is perfectly fine.



Please contact us again at ***@soe.ucsc.edu if you have any further
questions.



---

Steve Heitner

UCSC Genome Bioinformatics Group



From: Edge Edge [mailto:***@yahoo.com]
Sent: Tuesday, June 26, 2012 8:37 PM
To: ***@soe.ucsc.edu; ***@soe.ucsc.edu
Subject: Re: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from
UCSC Genome Browser



Dear Professor,
hg19_knownGene_uc010nxq.1 range=chr1:11874-12189 5'pad=0 3'pad=0 strand=+ repeatMasking=none
CTTGCCGTCAGCCTTTTCTTTGACCTCTTCTTTCTGTTCATGTGTATTTG
CTGTCTCTTAGCCCAGACTTCCCGTGTCCTTTCCACCGGGCCTTTGAGAG
GTCACAGGGTCTTGATGCTGTGGTCTTCATCTGCAGGTGTCTGACTTCCA
GCAACTGCTGGCCTGTGCCAGGGTGCAAGCTGAGCACTGGAGTGGAGTTT
TCCTGTGGAGAGGAGCCATGCCTAGAGTGGGATGGGCCATTGTTCATCTT
CTGGCCCCTGTTGTCTGCATGTAACTTAATACCACAACCAGGCATAGGGG
AAAGATTGGAGGAAAG
hg19_knownGene_uc001aaa.3 range=chr1:11874-14409 5'pad=0 3'pad=0 strand=+ repeatMasking=none
CTTGCCGTCAGCCTTTTCTTTGACCTCTTCTTTCTGTTCATGTGTATTTG
CTGTCTCTTAGCCCAGACTTCCCGTGTCCTTTCCACCGGGCCTTTGAGAG
GTCACAGGGTCTTGATGCTGTGGTCTTCATCTGCAGGTGTCTGACTTCCA
GCAACTGCTGGCCTGTGCCAGGGTGCAAGCTGAGCACTGGAGTGGAGTTT
TCCTGTGGAGAGGAGCCATGCCTAGAGTGGGATGGGCCATTGTTCATCTT
CTGGCCCCTGTTGTCTGCATGTAACTTAATACCACAACCAGGCATAGGGG
AAAGATTGGAGGAAAGATGAGTGAGAGCATCAACTTCTCTCACAACCTAG
GCCAGTGTGTGGTGATGCCAGGCATGCCCTTCCCCAGCATCAGGTCTCCA
GAGCTGCAGAAGACGACGGCCGACTTGGATCACACTCTTGTGAGTGTCCC
CAGTGTTGCAGAGGCAGGGCCATCAGGCACCAAAGGGATTCTGCCAGCAT
AGTGCTCCTGGACCAGTGATACACCCGGCACCCTGTCCTGGACACGCTGT
TGGCCTGGATCTGAGCCCTGGTGGAGGTCAAAGCCACCTTTGGTTCTGCC
ATTGCTGCTGTGTGGAAGTTCACTCCTGCCTTTTCCTTTCCCTAGAGCCT
CCACCACCCCGAGATCACATTTCTCACTGCCTTTTGTCTGCCCAGTTTCA
CCAGAAGTAGGCCTCTTCCTGACAGGCAGCTGCACCACTGCCTGGCGCTG
TGCCCTTCCTTTGCTCTGCCCGCTGGAGACGGTGTTTGTCATGGGCCTGG
TCTGCAGGGATCCTGCTACAAAGGTGAAACCCAGGAGAGTGTGGAGTCCA
GAGTGTTGCCAGGACCCAGGCACAGGCATTAGTGCCCGTTGGAGAAAACA
GGGGAATCCCGAAGAAATGGTGGGTCCTGGCCATCCGTGAGATCTTCCCA
GGGCAGCTCCCCTCTGTGGAATCCAATCTGTCTTCCATCCTGCGTGGCCG
AGGGCCAGGCTTCTCACTGGGCCTCTGCAGGAGGCTGCCATTTGTCCTGC
CCACCTTCTTAGAAGCGAGACGGAGCAGACCCATCTGCTACTGCCCTTTC
TATAATAACTAAAGTTAGCTGCCCTGGACTATTCACCCCCTAGTCTCAAT
TTAAGAAGATCCCCATGGCCACAGGGCCCCTGCCTGGGGGCTTGTCACCT
CCCCCACCTTCTTCCTGAGTCATTCCTGCAGCCTTGCTCCCTAACCTGCC
CCACAGCCTTGCCTGGATTTCTATCTCCCTGGCTTGGTGCCAGTTCCTCC
AAGTCGATGGCACCTCCCTCCCTCTCAACCACTTGAGCAAACTCCAAGAC
ATCTTCTACCCCAACACCAGCAATTGTGCCAAGGGCCATTAGGCTCTCAG
CATGACTATTTTTAGAGACCCCGTGTCTGTCACTGAAACCTTTTTTGTGG
GAGACTATTCCTCCCATCTGCAACAGCTGCCCCTGCTGACTGCCCTTCTC
TCCTCCCTCTCATCCCAGAGAAACAGGTCAGCTGGGAGCTTCTGCCCCCA
CTGCCTAGGGACCAACAGGGGCAGGAGGCAGTCACTGACCCCGAGACGTT
TGCATCCTGCACAGCTAGAGATCCTTTATTAAAAGCACACTGTTGGTTTC
TG

My problem is that how come 3'-UTR and 5'-UTR can be at the same region in
human genome?

Do you have any distinguish which part is the 3'-UTR and 5'-UTR?

Based on my understanding, the human genome structure should be
promoter-5'-UTR-exon-intron-3'UTR-terminator

Thus I confused that the region of 3'-UTR and 5'-UTR is fall within the same
region.



Many thanks for advice to solve my doubts.



best regards

Edge

Research Student



_____

From: Steve Heitner <***@soe.ucsc.edu>
To: 'Edge Edge' <***@yahoo.com>; ***@soe.ucsc.edu
Sent: Wednesday, June 27, 2012 2:16 AM
Subject: RE: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from
UCSC Genome Browser


Hello, Edge.

I repeated the steps you provided and I did not encounter a discrepancy
between the coordinates of the two queries. I would also like to add that
you do not need to set "group" to "All Tables" in order to use the rmsk
table. You can set "group" to "Variation and Repeats" and set "track" to
"RepeatMasker".

If you would like the coordinates of 5' UTR and 3' UTR regions, you will
need to use a gene track like UCSC Genes or RefSeq Genes. You can do so by
performing the following steps:

1. Set the following options:
Group: Genes and Gene Prediction Tracks
Track: UCSC Genes
Table: knownGene
Output format: sequence

2. Click the "get output" button

3. Select "genomic" and click the "submit" button

4. Check the "5' UTR Exons" and "3' UTR Exons" checkboxes and select any
other options you desire

5. Click the "get sequence" button

Note that the output here will not distinguish 5' UTR sequences from 3' UTR
sequences. If you want to distinguish 5' UTR sequences from 3' UTR
sequences, you will want to make two separate queries.

Please contact us again at ***@soe.ucsc.edu if you have any further
questions.

---
Steve Heitner
UCSC Genome Bioinformatics Group

-----Original Message-----
From: genome-***@soe.ucsc.edu [mailto:genome-***@soe.ucsc.edu] On
Behalf Of Edge Edge
Sent: Tuesday, June 26, 2012 8:41 AM
To: ***@soe.ucsc.edu
Cc: genome-***@soe.ucsc.edu
Subject: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from UCSC
Genome Browser

Dear Professor,
Can I know that how to extract the information (such as chromosome number,
position start and position ) of human hg19 3'-UTR, 5'-UTR, rRNA, tRNA
from UCSC Genome Browser?

I got extract rRNA and tRNA by using the following method:
* Select "All Tables" from the group drop-down list
* Select the "rmsk" table from the table drop-down list
* Choose "GTF" as the output format / Choose "Sequence" as the
output format
* Type a filename in "output file" so your browser downloads the
result
* Click "create" next to filter
* Next to "repClass," type rRNA
* Next to free-form query, select "OR" and type repClass = "tRNA"
* Click submit on that page, then get output on the main page

However, when I check the position of rRNA and tRNA in GTF format and
Sequence format.
It shown difference nucleotide.
Can I know how to solve this issue?
I just wanna to make sure the position of rRNA and tRNA in GTF format is
tally with the position and chromosome shown in Sequence format.
Can I know how to get all the info regarding human hg19 3'-UTR, 5'-UTR,
rRNA, tRNA from UCSC Genome Browser?

Many thanks for any advice.

best regards
Edge
Research Student
_______________________________________________
Genome maillist - ***@soe.ucsc.edu
https://lists.soe.ucsc.edu/mailman/listinfo/genome
Edge Edge
2012-06-29 01:08:34 UTC
Permalink
Dear Professor,

 
According your previous reply, "This is why you see overlap between the 5’ UTR of uc010nxq.1 and the 3’ UTR of uc001aaa.3 and this is perfectly fine."
In biology behaviour of human genome, is it normal that 3'-UTR overlap with 5'-UTR?
 
Can I know that whether UCSC got provide the coordinates of human miRNA?
If yes, can I know how to extract it out?
 
I got try to extract out the human exon coordinates by using the following method:
1. Set the following options:
Group: Genes and Gene Prediction Tracks
Track: RefSeq Genes
Table: knownGene
Output format: sequence

2. Click the "get output" button

3. Select "genomic" and click the "submit" button

4. Check the " CDS Exons " 

5. Click the "get sequence" button
 
From the result, it shown that 
hg19_refGene_NM_032291 range=chr1:67000042-67208778 5'pad=0 3'pad=0 strand=+ repeatMasking=none
However, when I check the coordinates through UCSC Genome Browser, it shown that chr1:67,000,042-67,208,778 is fall in Gene region but not exons of that particular gene.
 
Can I know how to just extract the coordinate of each exon in every gene?
My main purpose just hope can extract the coordinates of promoter, 3'-UTR, 5'-UTR, miRNA, rRNA, tRNA, exon position of human by using UCSC.
 
Really thanks for your advice.
Many thanks for your explanation in detail previously.
Very
helpful and learn a lot from your explanation.
I'm very fresh at bioinformatics.
 
Thanks.
 
best regards
Edge
Research Student  
_______________________________________________
Genome maillist - ***@soe.ucsc.edu
https://lists.
Brooke Rhead
2012-06-30 03:31:30 UTC
Permalink
Hi Edge,
perfectly fine." In biology behaviour of human genome, is it normal
that 3'-UTR overlap with 5'-UTR?
There is a bug in the Table Browser that I think is causing a lot of
confusion here. When you choose to retrieve 3' UTR or 5' UTR output
from a region where there is a non-coding gene, the Table Browser should
not return any result for that non-coding gene. We have recorded this
bug and we hope to fix it eventually. In the meantime, you will need
another way to distinguish UTRs from genes that are entirely non-coding.
Can I know that whether UCSC got provide the coordinates of human
miRNA? If yes, can I know how to extract it out?
There are several tracks that include miRNA annotations. To decide
which track you want to use, you can click on the track name on the main
Genome Browser page (http://genome.ucsc.edu/cgi-bin/hgTracks) and read
about where the data comes from and how recent it is. Some tracks you
might want to consider on hg19 are: sno/miRNA, tRNA Genes, RefSeq
Genes, UCSC Genes (which contains annotations based on data from RefSeq,
Genbank, CCDS, UniProt, Rfam, and the tRNA Genes track), and GENCODE.

To get coordinate positions, there is no need to retrieve sequence from
the Table Browser. There are two different ways to get coordinate
positions. The first is to choose either "all fields from selected
table" or "selected fields from primary and related tables" as the
output format. The start and stop coordinates will be included in the
output. Also, if the table includes UTRs (as in the refGene and
knownGene tables, for instance), you can calculate the positions of the
UTRs by subtracting txStart from cdsStart and cdsEnd from txEnd. (To
see a description of the fields of any table, select it in the Table
Browser and hit the "describe table schema" button.) To read more about
the way genome coordinates are stored in our tables, see:
http://genomewiki.ucsc.edu/index.php/Coordinate_Transforms.

The other way to get coordinate positions is to select the "BED -
browser extensible data" as the output format. BED format is described
here: http://genome.ucsc.edu/FAQ/FAQformat.html#format1. If you use
this method, you will be able to limit the output to just the UTRs.
However, you will run into the bug described above of completely
non-coding genes showing up in the output.

I hope this helps explain what you are seeing in the Genome Browser and
helps you get a start on using the Table Browser. If you haven't seen
the Open Helix tutorials on the Browser, especially the Table Browser
tutorial, you might find these helpful: http://www.openhelix.com/ucsc.

If you have further questions, please contact us again at
***@soe.ucsc.edu.

--
Brooke Rhead
UCSC Genome Bioinformatics Group
Dear Professor,
According your previous reply, "This is why you see overlap between
the 5’ UTR of uc010nxq.1 and the 3’ UTR of uc001aaa.3 and this is
perfectly fine." In biology behaviour of human genome, is it normal
that 3'-UTR overlap with 5'-UTR?
Can I know that whether UCSC got provide the coordinates of human
miRNA? If yes, can I know how to extract it out?
I got try to extract out the human exon coordinates by using the
following method: 1. Set the following options: Group: Genes and Gene
sequence
2. Click the "get output" button
3. Select "genomic" and click the "submit" button
4. Check the " CDS Exons "
5. Click the "get sequence" button
From the result, it shown that
hg19_refGene_NM_032291 range=chr1:67000042-67208778 5'pad=0 3'pad=0
strand=+ repeatMasking=none
However, when I check the coordinates through UCSC Genome Browser, it
shown that chr1:67,000,042-67,208,778 is fall in Gene region but not
exons of that particular gene.
Can I know how to just extract the coordinate of each exon in every
gene? My main purpose just hope can extract the coordinates of
promoter, 3'-UTR, 5'-UTR, miRNA, rRNA, tRNA, exon position of human
by using UCSC.
Really thanks for your advice. Many thanks for your explanation in
detail previously. Very helpful and learn a lot from your
explanation. I'm very fresh at bioinformatics.
Thanks.
best regards Edge Research Student
_______________________________________________ Genome maillist -
https://lists.soe.ucsc.edu/mailman/listinfo/genome
_______________________________________________
Genome maillist - ***@soe.ucsc.edu
Edge Edge
2012-07-02 01:36:43 UTC
Permalink
Dear Professor,

Many thanks for your reply and explanation.
I just download again the desired output in BED format through UCSC.
However, I still feel a bit with the following case:
Case 1:
Gene Name Chromosome Start Position End Position Remarks
PCDH15      10           55568451   55569239      3'UTR
PCDH15      10           55568451   55569306      coding exons
PCDH15      10           55568502   55568819      intron

It seems like PCDH15 is overlap based on UCSC output?
I can't really distinguish which regions is 3'UTR, coding exons or intron of PCDH15.

Case 2:
Gene Name Chromosome Start Position End Position Remarks
ATP5L      11           118279813   118280562      3'UTR
ATP5L      11           118279714   118280562      5'UTR

It will be good if you can provide which some real case to distinguish promoter region, 3'UTR, coding exons, 5'UTR and intron from the UCSC output result.


Thanks for your advice regarding miRNA, rRNA, tRNA, etc.
I able to solve it out now.

Looking forward to hear from you.

best regards
Edge




________________________________
From: Brooke Rhead <***@soe.ucsc.edu>
To: Edge Edge <***@yahoo.com>
Cc: ucsc <***@soe.ucsc.edu>
Sent: Saturday, June 30, 2012 11:31 AM
Subject: Re: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from UCSC Genome Browser

Hi Edge,
perfectly fine." In biology behaviour of human genome, is it normal
that 3'-UTR overlap with 5'-UTR?
There is a bug in the Table Browser that I think is causing a lot of confusion here.  When you choose to retrieve 3' UTR or 5' UTR output from a region where there is a non-coding gene, the Table Browser should not return any result for that non-coding gene.  We have recorded this bug and we hope to fix it eventually.  In the meantime, you will need another way to distinguish UTRs from genes that are entirely non-coding.
Can I know that whether UCSC got provide the coordinates of human
miRNA? If yes, can I know how to extract it out?
There are several tracks that include miRNA annotations.  To decide which track you want to use, you can click on the track name on the main Genome Browser page (http://genome.ucsc.edu/cgi-bin/hgTracks) and read about where the data comes from and how recent it is.  Some tracks you might want to consider on hg19 are:  sno/miRNA, tRNA Genes, RefSeq Genes, UCSC Genes (which contains annotations based on data from RefSeq, Genbank, CCDS, UniProt, Rfam, and the tRNA Genes track), and GENCODE.

To get coordinate positions, there is no need to retrieve sequence from the Table Browser.  There are two different ways to get coordinate positions.  The first is to choose either "all fields from selected table" or "selected fields from primary and related tables" as the output format.  The start and stop coordinates will be included in the output.  Also, if the table includes UTRs (as in the refGene and knownGene tables, for instance), you can calculate the positions of the UTRs by subtracting txStart from cdsStart and cdsEnd from txEnd.  (To see a description of the fields of any table, select it in the Table Browser and hit the "describe table schema" button.)  To read more about the way genome coordinates are stored in our tables, see: http://genomewiki.ucsc.edu/index.php/Coordinate_Transforms.

The other way to get coordinate positions is to select the "BED - browser extensible data" as the output format.  BED format is described here:  http://genome.ucsc.edu/FAQ/FAQformat.html#format1.  If you use this method, you will be able to limit the output to just the UTRs. However, you will run into the bug described above of completely non-coding genes showing up in the output.

I hope this helps explain what you are seeing in the Genome Browser and helps you get a start on using the Table Browser.  If you haven't seen the Open Helix tutorials on the Browser, especially the Table Browser tutorial, you might find these helpful:  http://www.openhelix.com/ucsc.

If you have further questions, please contact us again at ***@soe.ucsc.edu.

--
Brooke Rhead
UCSC Genome Bioinformatics Group
Dear Professor,
According your previous reply, "This is why you see overlap between
the 5’ UTR of uc010nxq.1 and the 3’ UTR of uc001aaa.3 and this is
perfectly fine." In biology behaviour of human genome, is it normal
that 3'-UTR overlap with 5'-UTR?
Can I know that whether UCSC got provide the coordinates of human
miRNA? If yes, can I know how to extract it out?
I got try to extract out the human exon coordinates by using the
following method: 1. Set the following options: Group: Genes and Gene
sequence
2. Click the "get output" button
3. Select "genomic" and click the "submit" button
4. Check the " CDS Exons "
5. Click the "get sequence" button
From the result, it shown that
hg19_refGene_NM_032291 range=chr1:67000042-67208778 5'pad=0 3'pad=0
strand=+ repeatMasking=none
However, when I check the coordinates through UCSC Genome Browser, it
shown that chr1:67,000,042-67,208,778 is fall in Gene region but not
exons of that particular gene.
Can I know how to just extract the coordinate of each exon in every
gene? My main purpose just hope can extract the coordinates of
promoter, 3'-UTR, 5'-UTR, miRNA, rRNA, tRNA, exon position of human
by using UCSC.
Really thanks for your advice. Many thanks for your explanation in
detail previously. Very helpful and learn a lot from your
explanation. I'm very fresh at bioinformatics.
Thanks.
best regards Edge Research Student
_______________________________________________ Genome maillist  -
https://lists.soe.ucsc.edu/mailman/listinfo/genome
_______________________________________________
Genome maillist - ***@soe.ucsc.edu
https://lists.soe.ucsc.edu/mailman/listi
Greg Roe
2012-07-10 19:07:04 UTC
Permalink
Hi,

Please take a look at PCDH15 in the genome browser:
http://genome.ucsc.edu/cgi-bin/hgTracks?clade=mammal&org=Human&db=hg19&position=chr10%3A55580860-56561051

You can see that there are many transcripts for this gene, each with
it's own id (e.g., uc010qhq.2, uc010qhr.2). I think maybe you're seeing
more than one transcript. If that's not the case, please let me know
how you are producing your output (what settings and steps in the Table
Browser?). Make sure you're getting the transcript name (from knownGenes
if you're using UCSC Genes) in your output.

Please let us know if you have any additional questions: ***@soe.ucsc.edu

-
Greg Roe
UCSC Genome Bioinformatics Group
Post by Edge Edge
Dear Professor,
Many thanks for your reply and explanation.
I just download again the desired output in BED format through UCSC.
Gene Name Chromosome Start Position End Position Remarks
PCDH15 10 55568451 55569239 3'UTR
PCDH15 10 55568451 55569306 coding exons
PCDH15 10 55568502 55568819 intron
It seems like PCDH15 is overlap based on UCSC output?
I can't really distinguish which regions is 3'UTR, coding exons or intron of PCDH15.
Gene Name Chromosome Start Position End Position Remarks
ATP5L 11 118279813 118280562 3'UTR
ATP5L 11 118279714 118280562 5'UTR
It will be good if you can provide which some real case to distinguish promoter region, 3'UTR, coding exons, 5'UTR and intron from the UCSC output result.
Thanks for your advice regarding miRNA, rRNA, tRNA, etc.
I able to solve it out now.
Looking forward to hear from you.
best regards
Edge
________________________________
Sent: Saturday, June 30, 2012 11:31 AM
Subject: Re: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from UCSC Genome Browser
Hi Edge,
perfectly fine." In biology behaviour of human genome, is it normal
that 3'-UTR overlap with 5'-UTR?
There is a bug in the Table Browser that I think is causing a lot of confusion here. When you choose to retrieve 3' UTR or 5' UTR output from a region where there is a non-coding gene, the Table Browser should not return any result for that non-coding gene. We have recorded this bug and we hope to fix it eventually. In the meantime, you will need another way to distinguish UTRs from genes that are entirely non-coding.
Can I know that whether UCSC got provide the coordinates of human
miRNA? If yes, can I know how to extract it out?
There are several tracks that include miRNA annotations. To decide which track you want to use, you can click on the track name on the main Genome Browser page (http://genome.ucsc.edu/cgi-bin/hgTracks) and read about where the data comes from and how recent it is. Some tracks you might want to consider on hg19 are: sno/miRNA, tRNA Genes, RefSeq Genes, UCSC Genes (which contains annotations based on data from RefSeq, Genbank, CCDS, UniProt, Rfam, and the tRNA Genes track), and GENCODE.
To get coordinate positions, there is no need to retrieve sequence from the Table Browser. There are two different ways to get coordinate positions. The first is to choose either "all fields from selected table" or "selected fields from primary and related tables" as the output format. The start and stop coordinates will be included in the output. Also, if the table includes UTRs (as in the refGene and knownGene tables, for instance), you can calculate the positions of the UTRs by subtracting txStart from cdsStart and cdsEnd from txEnd. (To see a description of the fields of any table, select it in the Table Browser and hit the "describe table schema" button.) To read more about the way genome coordinates are stored in our tables, see: http://genomewiki.ucsc.edu/index.php/Coordinate_Transforms.
The other way to get coordinate positions is to select the "BED - browser extensible data" as the output format. BED format is described here: http://genome.ucsc.edu/FAQ/FAQformat.html#format1. If you use this method, you will be able to limit the output to just the UTRs. However, you will run into the bug described above of completely non-coding genes showing up in the output.
I hope this helps explain what you are seeing in the Genome Browser and helps you get a start on using the Table Browser. If you haven't seen the Open Helix tutorials on the Browser, especially the Table Browser tutorial, you might find these helpful: http://www.openhelix.com/ucsc.
--
Brooke Rhead
UCSC Genome Bioinformatics Group
Dear Professor,
According your previous reply, "This is why you see overlap between
the 5’ UTR of uc010nxq.1 and the 3’ UTR of uc001aaa.3 and this is
perfectly fine." In biology behaviour of human genome, is it normal
that 3'-UTR overlap with 5'-UTR?
Can I know that whether UCSC got provide the coordinates of human
miRNA? If yes, can I know how to extract it out?
I got try to extract out the human exon coordinates by using the
following method: 1. Set the following options: Group: Genes and Gene
sequence
2. Click the "get output" button
3. Select "genomic" and click the "submit" button
4. Check the " CDS Exons "
5. Click the "get sequence" button
From the result, it shown that
hg19_refGene_NM_032291 range=chr1:67000042-67208778 5'pad=0 3'pad=0
strand=+ repeatMasking=none
However, when I check the coordinates through UCSC Genome Browser, it
shown that chr1:67,000,042-67,208,778 is fall in Gene region but not
exons of that particular gene.
Can I know how to just extract the coordinate of each exon in every
gene? My main purpose just hope can extract the coordinates of
promoter, 3'-UTR, 5'-UTR, miRNA, rRNA, tRNA, exon position of human
by using UCSC.
Really thanks for your advice. Many thanks for your explanation in
detail previously. Very helpful and learn a lot from your
explanation. I'm very fresh at bioinformatics.
Thanks.
best regards Edge Research Student
_______________________________________________ Genome maillist -
https://lists.soe.ucsc.edu/mailman/listinfo/genome
_______________________________________________
https://lists.soe.ucsc.edu/mailman/listinfo/genome
_______________________________________________
Genome maillist - ***@soe.ucsc.edu
https://lists.soe.u

Edge Edge
2012-06-27 02:35:21 UTC
Permalink
Dear Professor,
hg19_knownGene_uc001aaa.3 range=chr1:12228-13220 5'pad=0 3'pad=0 strand=+ repeatMasking=none
gtaagtagtgcttgtgctcatctccttggctgtgatacgtggccggccct
cgctccagcagctggacccctacctgccgtctgctgccatcggagcccaa
agccgggctgtgactgctcagaccagccggctggagggaggggctcagca
ggtctggctttggccctgggagagcaggtggaagatcaggcaggccatcg
ctgccacagaacccagtggattggcctaggtgggatctctgagctcaaca
agccctctctgggtggtaggtgcagagacgggaggggcagagccgcaggc
acagccaagagggctgaagaaatggtagaacggagcagctggtgatgtgt
gggcccaccggccccaggctcctgtctccccccaggtgagaggagagtag
acagtgagtgggagtggcgtcgcccctagggctctacggggccggcgtct
cctgtctcctggagaggcttcgatgcccctccacaccctcttgatcttcc
ctgtgatgtcatctggagccctgctgcttgcggtggcctataaagcctcc
tagtctggctccaaggcctggcagagtctttcccagggaaagctacaagc
agcaaacagtctgcatgggtcatccccttcactcccagctcagagcccag
gccaggggcccccaagaaaggctctggtggagaacctgtgcatgaaggct
gtcaaccagtccataggcaagcctggctgcctccagctgggtcgacagac
aggggctggagaaggggagaagaggaaagtgaggttgcctgccctgtctc
ctacctgaggctgaggaaggagaaggggatgcactgttggggaggcagct
gtaactcaaagccttagcctctgttcccacgaag
hg19_knownGene_uc010nxr.1 range=chr1:12228-13220 5'pad=0 3'pad=0 strand=+ repeatMasking=none
gtaagtagtgcttgtgctcatctccttggctgtgatacgtggccggccct
cgctccagcagctggacccctacctgccgtctgctgccatcggagcccaa
agccgggctgtgactgctcagaccagccggctggagggaggggctcagca
ggtctggctttggccctgggagagcaggtggaagatcaggcaggccatcg
ctgccacagaacccagtggattggcctaggtgggatctctgagctcaaca
agccctctctgggtggtaggtgcagagacgggaggggcagagccgcaggc
acagccaagagggctgaagaaatggtagaacggagcagctggtgatgtgt
gggcccaccggccccaggctcctgtctccccccaggtgtgtggtgatgcc
aggcatgcccttccccaggtgagtgtccccagtgttgcagaggtgagagg
agagtagacagtgagtgggagtggcgtcgcccctagggctctacggggcc
ggcgtctcctgtctcctggagaggcttcgatgcccctccacaccctcttg
atcttccctgtgatgtcatctggagccctgctgcttgcggtggcctataa
agcctcctagtctggctccaaggcctggcagagtctttcccagggaaagc
tacaagcagcaaacagtctgcatgggtcatccccttcactcccagctcag
agcccaggccaggggcccccaagaaaggctctggtggagaacctgtgcat
gaaggctgtcaaccagtccataggcaagcctggctgcctccagctgggtc
gacagacaggggctggagaaggggagaagaggaaagtgaggttgcctgcc
ctgtctcctacctgaggctgaggaaggagaaggggatgcactgttgggga
ggcagctgtaactcaaagccttagcctctgttcccacgaag

Both of the records shown the range from chr1:12228-13220. However, when I check the nucleotide of  chr1:12228-13220 only  hg19_knownGene_uc010nxr.1 shown the exactly nucleotide match with the chr1:12228-13220.
Can I know how I can judge whether which records to use for my research purpose in order to identify the 3'-UTR, 5'-UTR, intron, rRNA, tRNA, etc.

Many thanks and looking forward from your advice.

best regards
Edge


From: Steve Heitner <***@soe.ucsc.edu>

To: 'Edge Edge' <***@yahoo.com>; ***@soe.ucsc.edu
Sent: Wednesday, June 27, 2012 2:16 AM
Subject: RE: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from UCSC Genome Browser

Hello, Edge.

I repeated the steps you provided and I did not encounter a discrepancy
between the coordinates of the two queries.  I would also like to add that
you do not need to set "group" to "All Tables" in order to use the rmsk
table.  You can set "group" to "Variation and Repeats" and set "track" to
"RepeatMasker".

If you would like the coordinates of 5' UTR and 3' UTR regions, you will
need to use a gene track like UCSC Genes or RefSeq Genes.  You can do so by
performing the following steps:

1. Set the following options:
Group: Genes and Gene Prediction Tracks
Track: UCSC Genes
Table: knownGene
Output format: sequence

2. Click the "get output" button

3. Select "genomic" and click the "submit" button

4. Check the "5' UTR Exons" and "3' UTR Exons" checkboxes and select any
other options you desire

5. Click the "get sequence" button

Note that the output here will not distinguish 5' UTR sequences from 3' UTR
sequences.  If you want to distinguish 5' UTR sequences from 3' UTR
sequences, you will want to make two separate queries.

Please contact us again at ***@soe.ucsc.edu if you have any further
questions.

---
Steve Heitner
UCSC Genome Bioinformatics Group

-----Original Message-----
From: genome-***@soe.ucsc.edu [mailto:genome-***@soe.ucsc.edu] On
Behalf Of Edge Edge
Sent: Tuesday, June 26, 2012 8:41 AM
To: ***@soe.ucsc.edu
Cc: genome-***@soe.ucsc.edu
Subject: [Genome] Help with extract rRNA, tRNA, 3'-UTR and 5'-UTR from UCSC
Genome Browser

Dear Professor,
Can I know that how to extract the information (such as chromosome number,
 position start and position ) of human hg19 3'-UTR,  5'-UTR, rRNA, tRNA
from UCSC Genome Browser?

I got extract rRNA and tRNA by using the following method:
    * Select "All Tables" from the group drop-down list
    * Select the "rmsk" table from the table drop-down list
    * Choose "GTF" as the output format / Choose "Sequence" as the
output format
    * Type a filename in "output file" so your browser downloads the
result
    * Click "create" next to filter
    * Next to "repClass," type rRNA
    * Next to free-form query, select "OR" and type repClass = "tRNA"
    * Click submit on that page, then get output on the main page

However, when I check the position of rRNA and tRNA in GTF format and
Sequence format.
It shown difference nucleotide.
Can I know how to solve this issue?
I just wanna to make sure the position of rRNA and tRNA in GTF format is
tally with the position and chromosome shown in Sequence format.
Can I know how to get all the info regarding human hg19 3'-UTR,  5'-UTR,
rRNA, tRNA from UCSC Genome Browser?

Many thanks for any advice.

best regards
Edge
Research Student 
_______________________________________________
Genome maillist  -  ***@soe.ucsc.edu
https://lists.soe.ucsc.edu/mailman/listinfo/genome
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