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Thread | Thread Starter | Forum | Replies | Last Post |
hg19 genome reference for short read mapping | yh253 | Bioinformatics | 4 | 12-29-2013 10:11 PM |
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#1 |
Senior Member
Location: Boston area Join Date: Nov 2007
Posts: 747
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http://www.plosone.org/article/fetch...esentation=PDF
Reference-Free Validation of Short Read Data Jan Schröder1,2*, James Bailey1,2, Thomas Conway2, Justin Zobel1,2 1 Department of Computer Science and Software Engineering, The University of Melbourne, Parkville, Victoria, Australia, 2 NICTA Victoria Research Laboratory, Parkville, Victoria, Australia Background High-throughput DNA sequencing techniques offer the ability to rapidly and cheaply sequence material such as whole genomes. However, the short-read data produced by these techniques can be biased or compromised at several stages in the sequencing process; the sources and properties of some of these biases are not always known. Accurate assessment of bias is required for experimental quality control, genome assembly, and interpretation of coverage results. An additional challenge is that, for new genomes or material from an unidentified source, there may be no reference available against which the reads can be checked. Results We propose analytical methods for identifying biases in a collection of short reads, without recourse to a reference. These, in conjunction with existing approaches, comprise a methodology that can be used to quantify the quality of a set of reads. Our methods involve use of three different measures: analysis of base calls; analysis of k-mers; and analysis of distributions of k-mers. We apply our methodology to wide range of short read data and show that, surprisingly, strong biases appear to be present. These include gross overrepresentation of some poly-base sequences, per-position biases towards some bases, and apparent preferences for some starting positions over others. Conclusions The existence of biases in short read data is known, but they appear to be greater and more diverse than identified in previous literature. Statistical analysis of a set of short reads can help identify issues prior to assembly or resequencing, and should help guide chemical or statistical methods for bias rectification. |
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#2 |
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Location: Boston Join Date: Feb 2008
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This is an interesting paper, and it would be more interesting if the authors could stratified the plots by read quality. I guess what is happening is the base caller makes consistent errors on weak bases. In addition, part of the bias comes from the GC bias.
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