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hg19 genome reference for short read mapping | yh253 | Bioinformatics | 4 | 12-29-2013 10:11 PM |
Short read benchmark data | GerryB | Bioinformatics | 5 | 11-27-2010 03:07 PM |
Reference-Free Validation of Short Read Data | krobison | Literature Watch | 1 | 09-23-2010 05:40 PM |
PubMed: ABySS: A parallel assembler for short read sequence data. | Newsbot! | Literature Watch | 0 | 03-03-2009 06:00 AM |
PubMed: Substantial biases in ultra-short read data sets from high-throughput DNA seq | Newsbot! | Literature Watch | 0 | 07-29-2008 06:10 AM |
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Reference-free validation of short read data. PLoS One. 2010;5(9):e12681 Authors: Schröder J, Bailey J, Conway T, Zobel J 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. PMID: 20877643 [PubMed - indexed for MEDLINE] More... |
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