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SsarahP started a topic Subchallenge 1 of the precisionFDA NCI-CPTAC Mislabeling Challenge ends 11/4!in GeneralSubchallenge 1 of the precisionFDA NCI-CPTAC Mislabeling Challenge ends 11/4!
The NCI-CPTAC Multi-omics Enabled Sample Mislabeling Correction Challenge encourages the development and evaluation of computational algorithms that can...
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"Multiplicity" in 2001 Pevzner EULER paper
I have a question about exactly how the multiplicity of an edge in the de Bruijn graph is determined. It seems that the multiplicity is simply the number...
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Any suggestion for Chip-Seq analysis?
Hi! All,
I'm a newbie for Chip-Seq analysis.
As you guys already know, there are a bunch of software to analyze Chip-Seq data,...
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Finding genome coverage using random reads
Thank you for looking at my question. I am trying to solve this homework question.
Consider the problem of sequencing genome by...
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De novo assembly of human genomes with massively parallel short read sequencing
http://genome.cshlp.org/content/earl...1.109.abstract
Next-generation massively parallel DNA sequencing technologies...
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The Algorithms used in Bowtie.
Recently,I was learning how to use bowtie,but there are a lot of parameters which i don't know how to set. So I study the BWT, FM index ,Suffix Array...
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Pipeline Illumina question
Hi,
I'm a new member and I have some questions about Illumina Pipeline GAII.
In Ilumina pipeline documentation there is...
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BFAST: Blat-like Fast Accurate Search Tool for Large-Scale Genome Resequencing
I would like to introduce seqanswers to BFAST. BFAST facilitates the fast and accurate mapping of short reads to reference sequences. Some advantages...