Literature DB >> 26323713

RASER: reads aligner for SNPs and editing sites of RNA.

Jaegyoon Ahn1, Xinshu Xiao1.   

Abstract

MOTIVATION: Accurate identification of genetic variants such as single-nucleotide polymorphisms (SNPs) or RNA editing sites from RNA-Seq reads is important, yet challenging, because it necessitates a very low false-positive rate in read mapping. Although many read aligners are available, no single aligner was specifically developed or tested as an effective tool for SNP and RNA editing prediction.
RESULTS: We present RASER, an accurate read aligner with novel mapping schemes and index tree structure that aims to reduce false-positive mappings due to existence of highly similar regions. We demonstrate that RASER shows the best mapping accuracy compared with other popular algorithms and highest sensitivity in identifying multiply mapped reads. As a result, RASER displays superb efficacy in unbiased mapping of the alternative alleles of SNPs and in identification of RNA editing sites.
AVAILABILITY AND IMPLEMENTATION: RASER is written in C++ and freely available for download at https://github.com/jaegyoonahn/RASER.
© The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

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Year:  2015        PMID: 26323713      PMCID: PMC4692970          DOI: 10.1093/bioinformatics/btv505

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  27 in total

1.  BLAT--the BLAST-like alignment tool.

Authors:  W James Kent
Journal:  Genome Res       Date:  2002-04       Impact factor: 9.043

2.  Accurate identification of A-to-I RNA editing in human by transcriptome sequencing.

Authors:  Jae Hoon Bahn; Jae-Hyung Lee; Gang Li; Christopher Greer; Guangdun Peng; Xinshu Xiao
Journal:  Genome Res       Date:  2011-09-29       Impact factor: 9.043

Review 3.  Genome-wide allele-specific analysis: insights into regulatory variation.

Authors:  Tomi Pastinen
Journal:  Nat Rev Genet       Date:  2010-06-22       Impact factor: 53.242

4.  Comparative analysis of RNA-Seq alignment algorithms and the RNA-Seq unified mapper (RUM).

Authors:  Gregory R Grant; Michael H Farkas; Angel D Pizarro; Nicholas F Lahens; Jonathan Schug; Brian P Brunk; Christian J Stoeckert; John B Hogenesch; Eric A Pierce
Journal:  Bioinformatics       Date:  2011-07-19       Impact factor: 6.937

5.  Identification of common molecular subsequences.

Authors:  T F Smith; M S Waterman
Journal:  J Mol Biol       Date:  1981-03-25       Impact factor: 5.469

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.  A framework for variation discovery and genotyping using next-generation DNA sequencing data.

Authors:  Mark A DePristo; Eric Banks; Ryan Poplin; Kiran V Garimella; Jared R Maguire; Christopher Hartl; Anthony A Philippakis; Guillermo del Angel; Manuel A Rivas; Matt Hanna; Aaron McKenna; Tim J Fennell; Andrew M Kernytsky; Andrey Y Sivachenko; Kristian Cibulskis; Stacey B Gabriel; David Altshuler; Mark J Daly
Journal:  Nat Genet       Date:  2011-04-10       Impact factor: 38.330

8.  Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing.

Authors:  Graham A Heap; Jennie H M Yang; Kate Downes; Barry C Healy; Karen A Hunt; Nicholas Bockett; Lude Franke; Patrick C Dubois; Charles A Mein; Richard J Dobson; Thomas J Albert; Matthew J Rodesch; David G Clayton; John A Todd; David A van Heel; Vincent Plagnol
Journal:  Hum Mol Genet       Date:  2010-01-01       Impact factor: 6.150

9.  Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data.

Authors:  Jacob F Degner; John C Marioni; Athma A Pai; Joseph K Pickrell; Everlyne Nkadori; Yoav Gilad; Jonathan K Pritchard
Journal:  Bioinformatics       Date:  2009-10-06       Impact factor: 6.937

10.  TopHat: discovering splice junctions with RNA-Seq.

Authors:  Cole Trapnell; Lior Pachter; Steven L Salzberg
Journal:  Bioinformatics       Date:  2009-03-16       Impact factor: 6.937

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  12 in total

Review 1.  Single-nucleotide variants in human RNA: RNA editing and beyond.

Authors:  Yan Guo; Hui Yu; David C Samuels; Wei Yue; Scott Ness; Ying-Yong Zhao
Journal:  Brief Funct Genomics       Date:  2019-02-14       Impact factor: 4.241

2.  Selective Enrichment of A-to-I Edited Transcripts from Cellular RNA Using Endonuclease V.

Authors:  Steve D Knutson; Robert A Arthur; H Richard Johnston; Jennifer M Heemstra
Journal:  J Am Chem Soc       Date:  2020-03-05       Impact factor: 15.419

3.  RED-ML: a novel, effective RNA editing detection method based on machine learning.

Authors:  Heng Xiong; Dongbing Liu; Qiye Li; Mengyue Lei; Liqin Xu; Liang Wu; Zongji Wang; Shancheng Ren; Wangsheng Li; Min Xia; Lihua Lu; Haorong Lu; Yong Hou; Shida Zhu; Xin Liu; Yinghao Sun; Jian Wang; Huanming Yang; Kui Wu; Xun Xu; Leo J Lee
Journal:  Gigascience       Date:  2017-05-01       Impact factor: 6.524

4.  EndoVIPER-seq for Improved Detection of A-to-I Editing Sites in Cellular RNA.

Authors:  Steve D Knutson; Jennifer M Heemstra
Journal:  Curr Protoc Chem Biol       Date:  2020-06

5.  Gaining comprehensive biological insight into the transcriptome by performing a broad-spectrum RNA-seq analysis.

Authors:  Sayed Mohammad Ebrahim Sahraeian; Marghoob Mohiyuddin; Robert Sebra; Hagen Tilgner; Pegah T Afshar; Kin Fai Au; Narges Bani Asadi; Mark B Gerstein; Wing Hung Wong; Michael P Snyder; Eric Schadt; Hugo Y K Lam
Journal:  Nat Commun       Date:  2017-07-05       Impact factor: 14.919

6.  RNA editing in nascent RNA affects pre-mRNA splicing.

Authors:  Yun-Hua Esther Hsiao; Jae Hoon Bahn; Yun Yang; Xianzhi Lin; Stephen Tran; Ei-Wen Yang; Giovanni Quinones-Valdez; Xinshu Xiao
Journal:  Genome Res       Date:  2018-05-03       Impact factor: 9.043

7.  Structure-mediated modulation of mRNA abundance by A-to-I editing.

Authors:  Anneke Brümmer; Yun Yang; Tracey W Chan; Xinshu Xiao
Journal:  Nat Commun       Date:  2017-11-02       Impact factor: 14.919

8.  Widespread RNA editing dysregulation in brains from autistic individuals.

Authors:  Stephen S Tran; Hyun-Ik Jun; Jae Hoon Bahn; Adel Azghadi; Gokul Ramaswami; Eric L Van Nostrand; Thai B Nguyen; Yun-Hua E Hsiao; Changhoon Lee; Gabriel A Pratt; Verónica Martínez-Cerdeño; Randi J Hagerman; Gene W Yeo; Daniel H Geschwind; Xinshu Xiao
Journal:  Nat Neurosci       Date:  2018-12-17       Impact factor: 24.884

9.  Regulation of RNA editing by RNA-binding proteins in human cells.

Authors:  Giovanni Quinones-Valdez; Stephen S Tran; Hyun-Ik Jun; Jae Hoon Bahn; Ei-Wen Yang; Lijun Zhan; Anneke Brümmer; Xintao Wei; Eric L Van Nostrand; Gabriel A Pratt; Gene W Yeo; Brenton R Graveley; Xinshu Xiao
Journal:  Commun Biol       Date:  2019-01-14

10.  Hypothalamic transcriptomes of 99 mouse strains reveal trans eQTL hotspots, splicing QTLs and novel non-coding genes.

Authors:  Yehudit Hasin-Brumshtein; Arshad H Khan; Farhad Hormozdiari; Calvin Pan; Brian W Parks; Vladislav A Petyuk; Paul D Piehowski; Anneke Brümmer; Matteo Pellegrini; Xinshu Xiao; Eleazar Eskin; Richard D Smith; Aldons J Lusis; Desmond J Smith
Journal:  Elife       Date:  2016-09-13       Impact factor: 8.140

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