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Thread | Thread Starter | Forum | Replies | Last Post |
a basic question about coverage | maria_mari | Bioinformatics | 7 | 01-30-2012 04:12 PM |
some basic queries (mapping) | seq_lover | Genomic Resequencing | 0 | 11-18-2011 08:46 AM |
basic question about read groups | efoss | Bioinformatics | 2 | 10-19-2011 05:32 PM |
Basic Seq Soft | ednot | General | 1 | 05-02-2011 06:42 PM |
depth of coverage basic question | madsaan | Bioinformatics | 0 | 03-24-2011 07:40 AM |
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#1 |
Junior Member
Location: Kolkata Join Date: Feb 2012
Posts: 1
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I started working on whole genome sequencing and exome sequencing with Illumina HiSeq 2000 and also with 454 sequencer. Can anybody please help me to understand the data analysis of the sequenced reads????
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#2 |
Senior Member
Location: Boston area Join Date: Nov 2007
Posts: 747
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If you'd like answers to such a question, you should start by posting in the correct forum. Then, explain what you want to do with the reads. You're query can be condensed to "I ran an experiment; how do I analyze it?", and nobody can really help you without some real detail.
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#3 |
Member
Location: Alaska Join Date: Jan 2012
Posts: 49
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Anyone remember the days were you just dumped 3 volumes of Maniatis on a student desk and turned around... probably not.
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#4 |
--Site Admin--
Location: SF Bay Area, CA, USA Join Date: Oct 2007
Posts: 1,358
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Moved this to a new thread...and I really encourage the original poster to read the following:
http://www.ploscompbiol.org/article/...l.pcbi.1002202 |
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