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Thread | Thread Starter | Forum | Replies | Last Post |
Newbie Question: Calculating physical coverage from genome coverage | tristanstoeber | Illumina/Solexa | 4 | 06-24-2013 11:53 AM |
calculating the coverage over a gene | kjaja | Bioinformatics | 3 | 06-01-2012 07:01 AM |
calculating the coverage | lyz1030 | Bioinformatics | 3 | 04-03-2012 06:03 PM |
what program can i use for calculating coverage? | dkrtndhkd | Bioinformatics | 2 | 02-03-2012 06:39 PM |
Gene list for calculating coverage | nseh | Bioinformatics | 1 | 05-22-2011 07:31 AM |
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#1 |
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Location: India Join Date: May 2012
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How can we calculate the coverage of Illumina paired end whole genome sequencing data using Waterman equation? Example data is given:
Total reads = 450,000,000 Read length = 101 Genome size = 3000000000
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http://www.illumina.com/Documents/pr...alculation.pdf
The Lander/Waterman equation is a method for computing coverage. The general equation is: C = LN / G • C stands for coverage • G is the haploid genome length • L is the read length • N is the number of reads So, if we take one lane of single read human sequence with v3 chemistry, we get C = (100 bp)*(189×10^6)/(3×10^9 bp) = 6.3 This tells us that each base in the genome will be sequenced between six and seven times on average. --------------------- Though take care whether the "total reads" number is really the number of all reads (read 1 + read 2) or actually the "total pair" number. In the first case, you can just do the equation, however if it's the latter then you need to C = 2*LN/G Last edited by lorendarith; 12-08-2012 at 10:03 AM. |
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#3 |
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How can we know whether it is total number or paired number?
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