Dear Galaxy
I found a bug in extracting FATSA sequence tool in galaxy.
I extracted sequence of this location chr10 123229360 123229525 fgfr2 0 -
hg18_chr10_123229360_123229525_-
GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC AGTGTTAAAACATGA
And I checked back in UCSC browser by pasting the same location. The sequences are completely different (hg18).
Could you please help me in this issue
Thanx Gireesh
On 09/17/2010 05:28 AM, gireesh bogu wrote:
Dear Galaxy
I found a bug in extracting FATSA sequence tool in galaxy.
I extracted sequence of this location chr10 123229360 123229525 fgfr2 0
hg18_chr10_123229360_123229525_-
GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC AGTGTTAAAACATGA
check the reverse complement of your sequence.....FGFR2 is on the reverse strand of chromosome 10
Hans
And I checked back in UCSC browser by pasting the same location. The sequences are completely different (hg18).
Could you please help me in this issue
Thanx Gireesh
galaxy-user mailing list galaxy-user@lists.bx.psu.edu http://lists.bx.psu.edu/listinfo/galaxy-user
I think that you have extracted the "+" strand for your comparison. Below is the "-" strand from UCSC hg18
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=+ repeatMasking=lower
TTCATGTTTTAACACTGCCGTTTATGTGTGGATACTGAGGAAGGCATGGT TCGTAAGGCATGGGGTCTGGAGAAAAAACAGAATCATCTCCTGAAGAACA AGAACTTCTTGTGTCAGGGTAACTAGGTGAATACTGTTCGAGAGGTTGGC TGAGGTCCAAGTATTC
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=- repeatMasking=lower
GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC AGTGTTAAAACATGAA
On 10-09-16 11:28 PM, "gireesh bogu" gireeshkbogu@gmail.com wrote:
Dear Galaxy
I found a bug in extracting FATSA sequence tool in galaxy.
I extracted sequence of this location chr10 123229360 123229525 fgfr2 0 -
hg18_chr10_123229360_123229525_-
GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC AGTGTTAAAACATGA
And I checked back in UCSC browser by pasting the same location. The sequences are completely different (hg18).
Could you please help me in this issue
Thanx Gireesh
Did you use Galxy FASTA tool ? or UCSC table browser? I used Galaxy I'm sure th sequence Galaxy gave is completely different from UCSC (Only antisense strand).
On Fri, Sep 17, 2010 at 7:08 PM, John McPherson John.McPherson@oicr.on.cawrote:
I think that you have extracted the “+” strand for your comparison. Below is the “-” strand from UCSC hg18
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=+
repeatMasking=lower TTCATGTTTTAACACTGCCGTTTATGTGTGGATACTGAGGAAGGCATGGT TCGTAAGGCATGGGGTCTGGAGAAAAAACAGAATCATCTCCTGAAGAACA AGAACTTCTTGTGTCAGGGTAACTAGGTGAATACTGTTCGAGAGGTTGGC TGAGGTCCAAGTATTC
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=-
repeatMasking=lower GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC
AGTGTTAAAACATGAA
On 10-09-16 11:28 PM, "gireesh bogu" gireeshkbogu@gmail.com wrote:
Dear Galaxy
I found a bug in extracting FATSA sequence tool in galaxy.
I extracted sequence of this location chr10 123229360 123229525 fgfr2 0 -
hg18_chr10_123229360_123229525_-
GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC AGTGTTAAAACATGA
And I checked back in UCSC browser by pasting the same location. The sequences are completely different (hg18).
Could you please help me in this issue
Thanx Gireesh
No I extrcated -. But your sense antisense sequences should be the same but in reverse right? But your two sequences are completely different ? Why is that?
On Fri, Sep 17, 2010 at 7:08 PM, John McPherson John.McPherson@oicr.on.cawrote:
I think that you have extracted the “+” strand for your comparison. Below is the “-” strand from UCSC hg18
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=+
repeatMasking=lower TTCATGTTTTAACACTGCCGTTTATGTGTGGATACTGAGGAAGGCATGGT TCGTAAGGCATGGGGTCTGGAGAAAAAACAGAATCATCTCCTGAAGAACA AGAACTTCTTGTGTCAGGGTAACTAGGTGAATACTGTTCGAGAGGTTGGC TGAGGTCCAAGTATTC
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=-
repeatMasking=lower GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC
AGTGTTAAAACATGAA
On 10-09-16 11:28 PM, "gireesh bogu" gireeshkbogu@gmail.com wrote:
Dear Galaxy
I found a bug in extracting FATSA sequence tool in galaxy.
I extracted sequence of this location chr10 123229360 123229525 fgfr2 0 -
hg18_chr10_123229360_123229525_-
GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC AGTGTTAAAACATGA
And I checked back in UCSC browser by pasting the same location. The sequences are completely different (hg18).
Could you please help me in this issue
Thanx Gireesh
Hey Gireesh,
The sequences are not just reverse but reverse complement, AND they are written ONLY in the 5' to 3' direction.
Taking the example of the first 16 bases ( in red) are the reverse complement of the last 16 ( in pink).
5'-3':TTCATGTTTTAACACT 5'-3':AGTGTTAAAACATGAA
Now flip the lower sequence around ( write is 3'-5' direction) and the beauty of the DNA strand becomes obvious with A's pairing with T and G with C
5'-3':TTCATGTTTTAACACT 3'-5':AAGTACAAAATTGTGA
On Fri, Sep 17, 2010 at 7:08 PM, John McPherson John.McPherson@oicr.on.ca wrote: I think that you have extracted the “+” strand for your comparison. Below is the “-” strand from UCSC hg18
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=+ repeatMasking=lower
TTCATGTTTTAACACTGCCGTTTATGTGTGGATACTGAGGAAGGCATGGT TCGTAAGGCATGGGGTCTGGAGAAAAAACAGAATCATCTCCTGAAGAACA AGAACTTCTTGTGTCAGGGTAACTAGGTGAATACTGTTCGAGAGGTTGGC TGAGGTCCAAGTATTC
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=- repeatMasking=lower
GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC AGTGTTAAAACATGAA
On Sep 17, 2010, at 5:52 PM, gireesh bogu wrote:
No I extrcated -. But your sense antisense sequences should be the same but in reverse right? But your two sequences are completely different ? Why is that?
On Fri, Sep 17, 2010 at 7:08 PM, John McPherson John.McPherson@oicr.on.ca wrote: I think that you have extracted the “+” strand for your comparison. Below is the “-” strand from UCSC hg18
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=+ repeatMasking=lower
TTCATGTTTTAACACTGCCGTTTATGTGTGGATACTGAGGAAGGCATGGT TCGTAAGGCATGGGGTCTGGAGAAAAAACAGAATCATCTCCTGAAGAACA AGAACTTCTTGTGTCAGGGTAACTAGGTGAATACTGTTCGAGAGGTTGGC TGAGGTCCAAGTATTC
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=- repeatMasking=lower
GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC AGTGTTAAAACATGAA
On 10-09-16 11:28 PM, "gireesh bogu" gireeshkbogu@gmail.com wrote:
Dear Galaxy
I found a bug in extracting FATSA sequence tool in galaxy.
I extracted sequence of this location chr10 123229360 123229525 fgfr2 0 -
hg18_chr10_123229360_123229525_-
GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC AGTGTTAAAACATGA
And I checked back in UCSC browser by pasting the same location. The sequences are completely different (hg18).
Could you please help me in this issue
Thanx Gireesh
galaxy-user mailing list galaxy-user@lists.bx.psu.edu http://lists.bx.psu.edu/listinfo/galaxy-user
Hi evrybody, I would like to align some sequences to maize genome. How I can import it to galaxy?. My sequences are already loaded and I have the "ZmB73_AGPv1_genome.fasta.gz" file (not loaded yet), but I'm not sure if is this
that I have to do. Any suggest are wellcome Best regards, Cristian
Cristian,
You can use your FASTA file with the NGS mappers (BWA, Bowtie, Lastz). Galaxy allows you to upload a gzipped file into your history, which it extracts after you upload it. Note that the file should be a single FASTA file containing all chromosomes/scaffolds/etc., each marked with a single header line. (Also, the file can only be gzipped (not tarred and gzipped)--it looks like yours is fine.) Then, when you are going to do the mapping, select the Use one from your history option instead of using one of the built-in indexes. Galaxy will create the indexes that the mapper needs from your supplied FASTA file before it does the mapping.
Let us know if you need any further assistance.
Regards, Kelly
On Sep 18, 2010, at 3:43 PM, Cristian Rojas wrote:
Hi evrybody, I would like to align some sequences to maize genome. How I can import it to galaxy?. My sequences are already loaded and I have the "ZmB73_AGPv1_genome.fasta.gz" file (not loaded yet), but I'm not sure if is this that I have to do. Any suggest are wellcome Best regards, Cristian
galaxy-user mailing list galaxy-user@lists.bx.psu.edu http://lists.bx.psu.edu/listinfo/galaxy-user
Hey Ruchi thanx for detailed explanation :)
cheers Gireesh
On Sat, Sep 18, 2010 at 10:46 PM, Ruchi Bajpai rbajpai@stanford.edu wrote:
Hey Gireesh,
The sequences are not just reverse but reverse complement, AND they are written ONLY in the 5' to 3' direction.
Taking the example of the first 16 bases ( in red) are the reverse complement of the last 16 ( in pink).
5'-3':TTCATGTTTTAACACT 5'-3':AGTGTTAAAACATGAA
Now flip the lower sequence around ( write is 3'-5' direction) and the beauty of the DNA strand becomes obvious with A's pairing with T and G with C
5'-3':TTCATGTTTTAACACT 3'-5':AAGTACAAAATTGTGA
On Fri, Sep 17, 2010 at 7:08 PM, John McPherson <John.McPherson@oicr.on.ca
wrote:
I think that you have extracted the “+” strand for your comparison. Below is the “-” strand from UCSC hg18
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=+
repeatMasking=lower TTCATGTTTTAACACTGCCGTTTATGTGTGGATACTGAGGAAGGCATGGT TCGTAAGGCATGGGGTCTGGAGAAAAAACAGAATCATCTCCTGAAGAACA AGAACTTCTTGTGTCAGGGTAACTAGGTGAATACTGTTCGAGAGGTTGGC TGAGGTCCAAGTATTC
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=-
repeatMasking=lower GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC AGTGTTAAAACATGAA
On Sep 17, 2010, at 5:52 PM, gireesh bogu wrote:
No I extrcated -. But your sense antisense sequences should be the same but in reverse right? But your two sequences are completely different ? Why is that?
On Fri, Sep 17, 2010 at 7:08 PM, John McPherson <John.McPherson@oicr.on.ca
wrote:
I think that you have extracted the “+” strand for your comparison. Below is the “-” strand from UCSC hg18
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=+
repeatMasking=lower TTCATGTTTTAACACTGCCGTTTATGTGTGGATACTGAGGAAGGCATGGT TCGTAAGGCATGGGGTCTGGAGAAAAAACAGAATCATCTCCTGAAGAACA AGAACTTCTTGTGTCAGGGTAACTAGGTGAATACTGTTCGAGAGGTTGGC TGAGGTCCAAGTATTC
hg18_dna range=chr10:123229360-123229525 5'pad=0 3'pad=0 strand=-
repeatMasking=lower GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC
AGTGTTAAAACATGAA
On 10-09-16 11:28 PM, "gireesh bogu" gireeshkbogu@gmail.com wrote:
Dear Galaxy
I found a bug in extracting FATSA sequence tool in galaxy.
I extracted sequence of this location chr10 123229360 123229525 fgfr2 0 -
hg18_chr10_123229360_123229525_-
GAATACTTGGACCTCAGCCAACCTCTCGAACAGTATTCACCTAGTTACCC TGACACAAGAAGTTCTTGTTCTTCAGGAGATGATTCTGTTTTTTCTCCAG ACCCCATGCCTTACGAACCATGCCTTCCTCAGTATCCACACATAAACGGC AGTGTTAAAACATGA
And I checked back in UCSC browser by pasting the same location. The sequences are completely different (hg18).
Could you please help me in this issue
Thanx Gireesh
galaxy-user mailing list galaxy-user@lists.bx.psu.edu http://lists.bx.psu.edu/listinfo/galaxy-user
galaxy-user@lists.galaxyproject.org
-
Cristian Rojas -
gireesh bogu -
Hans-Rudolf Hotz -
John McPherson -
Kelly Vincent -
Ruchi Bajpai