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Thread | Thread Starter | Forum | Replies | Last Post |
what is the best software to use to analyze illumina NGS data? | bbsinfo | Illumina/Solexa | 3 | 08-21-2013 05:48 AM |
Illumina HiSeq 2000 publication | vinay052003 | Illumina/Solexa | 1 | 11-07-2011 02:28 PM |
bowtie command line for Illumina Hiseq 2000 with Illumina 1.5+ quality encoding files | rworthi | Illumina/Solexa | 4 | 09-28-2011 12:25 PM |
Hiseq 2000 paired-end capture data analysis problem-too many variants! | lazyworm | Bioinformatics | 1 | 08-11-2010 11:03 AM |
Illumina's new sequencer: HiSeq 2000 | mccullou | Illumina/Solexa | 14 | 01-19-2010 12:08 PM |
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#1 |
Junior Member
Location: India Join Date: Dec 2011
Posts: 2
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Dear List,
I am new to NGS field. I have paired end sequenced Human Illumina HiSeq 2000 Data and have find SNP's out of that. And then I have to fidn out association of SNP's to a perticular trait. I would like to use open source tools such as bioconductor packages for data analysis. Hence, can somebody give me a functional pipeline for data analysis? Thanking you in anticipation. Regards, Kiradi |
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#2 |
Member
Location: Taiwan Join Date: Feb 2011
Posts: 19
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Dear kiradi,
You can try VarioWatch (http://genepipe.ncgm.sinica.edu.tw/variowatch/main.do) to see if it helps. It provides MegaQuery Download to download millions of annotated variants for NGS data in minutes. Adam |
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#3 |
Senior Member
Location: St. Louis Join Date: Dec 2010
Posts: 535
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Is it whole exome data? Regardless, you might want to read through this thread: http://seqanswers.com/forums/showthr...uencing+manual
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#4 | |
Junior Member
Location: India Join Date: Dec 2011
Posts: 2
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#5 |
Senior Member
Location: St. Louis Join Date: Dec 2010
Posts: 535
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It's not my documentation, haha.
A lot of those things are available freely to anybody. For example, type in "donwload GATK" into google and you'll find the right link. |
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