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Thread | Thread Starter | Forum | Replies | Last Post |
Count the Number of Paired-End Reads Mapped by Tophat | Fernas | Bioinformatics | 5 | 10-23-2015 03:26 AM |
Count number of reads in peaks? | albireo | Bioinformatics | 4 | 04-13-2013 07:51 PM |
How to count number of mapped paired-end and single-end rna-seq reads | repinementer | Bioinformatics | 8 | 01-06-2013 06:06 AM |
Count unique reads in a FASTQ file | id0 | Bioinformatics | 2 | 10-24-2012 02:01 AM |
cufflinks with collapsed reads files | SongLi | Bioinformatics | 0 | 11-19-2010 12:10 PM |
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#1 |
Member
Location: quebec Join Date: Apr 2013
Posts: 35
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Hi all,
I used bowtie to align a collapsed fasta file to the bovine genome and get a fasta file (mapped.fa) including all the mapped reads. But this mapped.fa is also a collapsed file. So how could I get the total reads number in mapped.fa, instead of the unique reads number? Thanks. Ran |
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#2 |
Senior Member
Location: St. Louis Join Date: Dec 2010
Posts: 535
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What do you mean by "collapsed"? Could you copy and paste the exact commands that were run?
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#3 |
Member
Location: quebec Join Date: Apr 2013
Posts: 35
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Hi Heisman, thanks for your reply. The collapsed file included the unique reads:
>1-30176523 TCAGTGCACTACAGAACTTTGT >2-17234938 TTCAAGTAATCCAGGATAGGCT >5-10273189 TACCCTGTAGAACCGAATTTGT >6-10202799 TGAGATGAAGCACTGTAGCT >7-7833696 TGAGATGAAGCACTGTAGCTCT >8-7677783 TGTAAACATCCTCGACTGGA >9-7403197 TGTAAACATCCTCGACTGGAAGCT >10-5760993 TGGGGGGCCCAAGTCCTTCTGATCGAGGCC So here I can get the number of total unique reads. But each unique read represents thousands of reads. How could I get the total number of the redundant reads in this file? Thanks! |
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