Wayne:High Throughput Sequencing Resources: Difference between revisions

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== High throughput (HT) datatypes and workflow ==
== High throughput (HT) datatypes and workflow ==


bcl file conversion to qseq <br>
File formats and conversions <br>
Qseq and fastq file conversions <br>
<ul>
Deplexing <br>
<li> bcl
Fastq inspection (quality) <br>
<li> qseq
<li> fastq
<li>
</ul>
<br>
Deplexing using barcoded sequence tags<br>
<ul>
<li> Editing (or hamming) distance
</ul>
<br>
Quality control <br>
<ul>
<li> Fastx tools
<li> Using mapping as the quality control for reads
</ul>
<br>
Trimming and clipping <br>
Trimming and clipping <br>
<br>
Assembly (by reference or de novo) <br>
Assembly (by reference or de novo) <br>
<br>
<u>Platform and read type</u><br>
<u>Platform and read type</u><br>
<ul>
<ul>
Line 34: Line 51:
<li> Genominator (Bullard et al. 2010)
<li> Genominator (Bullard et al. 2010)
</ul>
</ul>


== R basics ==
== R basics ==

Revision as of 16:48, 15 February 2013

High throughput (HT) datatypes and workflow

File formats and conversions

  • bcl
  • qseq
  • fastq


Deplexing using barcoded sequence tags

  • Editing (or hamming) distance


Quality control

  • Fastx tools
  • Using mapping as the quality control for reads


Trimming and clipping

Assembly (by reference or de novo)

Platform and read type

  • Illumina single-end vs. paired-end
  • 454 Roche
  • SOLiD
  • MiSeq
  • Ion Torrent

DNA sequence analysis


RNA-seq analysis

  • Quantifying and annotating aligned reads
  • DESeq
  • edgeR

A variety of additional R packages are available for normalizing RNA-Seq read count data and identifying differentially expressed genes (DEG):

  • easyRNASeq (simplifies read counting per genome feature)
  • DEXSeq (Inference of differential exon usage)
  • DEGseq
  • baySeq (also see: segmentSeq)
  • Genominator (Bullard et al. 2010)

R basics

HT sequence analysis using R (and Bioconductor)