Literature DB >> 29456282

Beta approximation of ratio distribution and its application to next generation sequencing read counts.

Shengping Yang1, Zhide Fang2.   

Abstract

Paired sequencing data are commonly collected in genomic studies to control biological variation. However, existing data processing strategies suffer at low coverage regions, which are unavoidable due to the limitation of current sequencing technology. Furthermore, information contained in the absolute values of the read counts is commonly ignored. We propose a read count ratio processing/modification method, to not only incorporate information contained in the absolute values of paired counts into one variable, but also mitigate the discrete artifact, especially when both counts are small. Simulation shows that the processed variable fits well with a Beta distribution, thus providing an easy tool for down-stream inference analysis.

Entities:  

Keywords:  Beta distribution; Next-generation sequencing; Paired tumor and normal tissues; Primary 62E17; Ratio of counts; Statistical artifacts; secondary 62P10

Year:  2016        PMID: 29456282      PMCID: PMC5812702          DOI: 10.1080/02664763.2016.1158798

Source DB:  PubMed          Journal:  J Appl Stat        ISSN: 0266-4763            Impact factor:   1.404


  10 in total

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Authors:  R David Hawkins; Gary C Hon; Bing Ren
Journal:  Nat Rev Genet       Date:  2010-07       Impact factor: 53.242

2.  PAIR: paired allelic log-intensity-ratio-based normalization method for SNP-CGH arrays.

Authors:  Shengping Yang; Stanley Pounds; Kun Zhang; Zhide Fang
Journal:  Bioinformatics       Date:  2012-11-29       Impact factor: 6.937

3.  The Sequence Alignment/Map format and SAMtools.

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Journal:  Bioinformatics       Date:  2009-06-08       Impact factor: 6.937

4.  rSW-seq: algorithm for detection of copy number alterations in deep sequencing data.

Authors:  Tae-Min Kim; Lovelace J Luquette; Ruibin Xi; Peter J Park
Journal:  BMC Bioinformatics       Date:  2010-08-18       Impact factor: 3.169

5.  High-resolution mapping of copy-number alterations with massively parallel sequencing.

Authors:  Derek Y Chiang; Gad Getz; David B Jaffe; Michael J T O'Kelly; Xiaojun Zhao; Scott L Carter; Carsten Russ; Chad Nusbaum; Matthew Meyerson; Eric S Lander
Journal:  Nat Methods       Date:  2008-11-30       Impact factor: 28.547

6.  Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.

Authors:  Ben Langmead; Cole Trapnell; Mihai Pop; Steven L Salzberg
Journal:  Genome Biol       Date:  2009-03-04       Impact factor: 13.583

7.  Comparison of methods to detect copy number alterations in cancer using simulated and real genotyping data.

Authors:  David Mosén-Ansorena; Ana María Aransay; Naiara Rodríguez-Ezpeleta
Journal:  BMC Bioinformatics       Date:  2012-08-07       Impact factor: 3.169

8.  Fractal-like distributions over the rational numbers in high-throughput biological and clinical data.

Authors:  Vladimir Trifonov; Laura Pasqualucci; Riccardo Dalla-Favera; Raul Rabadan
Journal:  Sci Rep       Date:  2011-12-13       Impact factor: 4.379

9.  CNV-seq, a new method to detect copy number variation using high-throughput sequencing.

Authors:  Chao Xie; Martti T Tammi
Journal:  BMC Bioinformatics       Date:  2009-03-06       Impact factor: 3.169

10.  WaveCNV: allele-specific copy number alterations in primary tumors and xenograft models from next-generation sequencing.

Authors:  Carson Holt; Bojan Losic; Deepa Pai; Zhen Zhao; Quang Trinh; Sujata Syam; Niloofar Arshadi; Gun Ho Jang; Johar Ali; Tim Beck; John McPherson; Lakshmi B Muthuswamy
Journal:  Bioinformatics       Date:  2013-11-04       Impact factor: 6.937

  10 in total
  1 in total

1.  Gene transcription changes in a locust model of noise-induced deafness.

Authors:  Andrew S French; Ben Warren
Journal:  J Neurophysiol       Date:  2021-05-05       Impact factor: 2.714

  1 in total

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