193 related articles for article (PubMed ID: 22496837)
1. Fast homozygosity mapping and identification of a zebrafish ENU-induced mutation by whole-genome sequencing.
Voz ML; Coppieters W; Manfroid I; Baudhuin A; Von Berg V; Charlier C; Meyer D; Driever W; Martial JA; Peers B
PLoS One; 2012; 7(4):e34671. PubMed ID: 22496837
[TBL] [Abstract][Full Text] [Related]
2. Rapid positional cloning of zebrafish mutations by linkage and homozygosity mapping using whole-genome sequencing.
Obholzer N; Swinburne IA; Schwab E; Nechiporuk AV; Nicolson T; Megason SG
Development; 2012 Nov; 139(22):4280-90. PubMed ID: 23052906
[TBL] [Abstract][Full Text] [Related]
3. Efficient mapping and cloning of mutations in zebrafish by low-coverage whole-genome sequencing.
Bowen ME; Henke K; Siegfried KR; Warman ML; Harris MP
Genetics; 2012 Mar; 190(3):1017-24. PubMed ID: 22174069
[TBL] [Abstract][Full Text] [Related]
4. Perspectives for identification of mutations in the zebrafish: making use of next-generation sequencing technologies for forward genetic approaches.
Henke K; Bowen ME; Harris MP
Methods; 2013 Aug; 62(3):185-96. PubMed ID: 23748111
[TBL] [Abstract][Full Text] [Related]
5. Mutation mapping and identification by whole-genome sequencing.
Leshchiner I; Alexa K; Kelsey P; Adzhubei I; Austin-Tse CA; Cooney JD; Anderson H; King MJ; Stottmann RW; Garnaas MK; Ha S; Drummond IA; Paw BH; North TE; Beier DR; Goessling W; Sunyaev SR
Genome Res; 2012 Aug; 22(8):1541-8. PubMed ID: 22555591
[TBL] [Abstract][Full Text] [Related]
6. An ENU-induced mutation in Rs1h causes disruption of retinal structure and function.
Jablonski MM; Dalke C; Wang X; Lu L; Manly KF; Pretsch W; Favor J; Pardue MT; Rinchik EM; Williams RW; Goldowitz D; Graw J
Mol Vis; 2005 Jul; 11():569-81. PubMed ID: 16088326
[TBL] [Abstract][Full Text] [Related]
7. [Positional cloning of a novel allele of zebrafish cloche mutant].
Ma N; Huo ZJ; Yan G; Huang HH; Luo SQ; Zhang WQ
Nan Fang Yi Ke Da Xue Xue Bao; 2010 Mar; 30(3):458-62. PubMed ID: 20335109
[TBL] [Abstract][Full Text] [Related]
8. An ENU mutagenesis screen in zebrafish for visual system mutants identifies a novel splice-acceptor site mutation in patched2 that results in Colobomas.
Lee J; Cox BD; Daly CM; Lee C; Nuckels RJ; Tittle RK; Uribe RA; Gross JM
Invest Ophthalmol Vis Sci; 2012 Dec; 53(13):8214-21. PubMed ID: 23150614
[TBL] [Abstract][Full Text] [Related]
9. Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice.
Geister KA; Timms AE; Beier DR
G3 (Bethesda); 2018 Feb; 8(2):401-409. PubMed ID: 29208648
[TBL] [Abstract][Full Text] [Related]
10. Identifying Toxicant-Interacting Genes Using Forward Genetic Screening in Zebrafish.
Hill JT
Methods Mol Biol; 2019; 1965():251-259. PubMed ID: 31069680
[TBL] [Abstract][Full Text] [Related]
11. Rapid identification and recovery of ENU-induced mutations with next-generation sequencing and Paired-End Low-Error analysis.
Pan L; Shah AN; Phelps IG; Doherty D; Johnson EA; Moens CB
BMC Genomics; 2015 Feb; 16(1):83. PubMed ID: 25886285
[TBL] [Abstract][Full Text] [Related]
12. Forward Genetic Screen Using Zebrafish to Identify New Genes Involved in Myelination.
Kegel L; Rubio M; Almeida RG; Benito S; Klingseisen A; Lyons DA
Methods Mol Biol; 2019; 1936():185-209. PubMed ID: 30820900
[TBL] [Abstract][Full Text] [Related]
13. Methods for reverse genetic screening in zebrafish by resequencing and TILLING.
Sood R; English MA; Jones M; Mullikin J; Wang DM; Anderson M; Wu D; Chandrasekharappa SC; Yu J; Zhang J; Paul Liu P
Methods; 2006 Jul; 39(3):220-7. PubMed ID: 16828311
[TBL] [Abstract][Full Text] [Related]
14. Genetic suppressor screens in haploids.
Bai X; Yang Z; Jiang H; Lin S; Zon LI
Methods Cell Biol; 2011; 104():129-36. PubMed ID: 21924160
[TBL] [Abstract][Full Text] [Related]
15. Whole Genome Sequencing-Based Mapping and Candidate Identification of Mutations from Fixed Zebrafish Tissue.
Sanchez NE; Harty BL; O'Reilly-Pol T; Ackerman SD; Herbert AL; Holmgren M; Johnson SL; Gray RS; Monk KR
G3 (Bethesda); 2017 Oct; 7(10):3415-3425. PubMed ID: 28855284
[TBL] [Abstract][Full Text] [Related]
16. Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis.
Damerla RR; Chatterjee B; Li Y; Francis RJ; Fatakia SN; Lo CW
Mamm Genome; 2014 Apr; 25(3-4):120-8. PubMed ID: 24306492
[TBL] [Abstract][Full Text] [Related]
17. High resolution mapping and positional cloning of ENU-induced mutations in the Rw region of mouse chromosome 5.
Ching YH; Munroe RJ; Moran JL; Barker AK; Mauceli E; Fennell T; Dipalma F; Lindblad-Toh K; Abcunas LM; Gilmour JF; Harris TP; Kloet SL; Luo Y; McElwee JL; Mu W; Park HK; Rogal DL; Schimenti KJ; Shen L; Shindo M; Shou JY; Stenson EK; Stover PJ; Schimenti JC
BMC Genet; 2010 Nov; 11():106. PubMed ID: 21118569
[TBL] [Abstract][Full Text] [Related]
18. Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy.
Zhang Z; Alpert D; Francis R; Chatterjee B; Yu Q; Tansey T; Sabol SL; Cui C; Bai Y; Koriabine M; Yoshinaga Y; Cheng JF; Chen F; Martin J; Schackwitz W; Gunn TM; Kramer KL; De Jong PJ; Pennacchio LA; Lo CW
Proc Natl Acad Sci U S A; 2009 Mar; 106(9):3219-24. PubMed ID: 19218456
[TBL] [Abstract][Full Text] [Related]
19. Rapid identification of a disease allele in mouse through whole genome sequencing and bulk segregation analysis.
Arnold CN; Xia Y; Lin P; Ross C; Schwander M; Smart NG; Müller U; Beutler B
Genetics; 2011 Mar; 187(3):633-41. PubMed ID: 21196518
[TBL] [Abstract][Full Text] [Related]
20. Molecular characterization of ENU mouse mutagenesis and archives.
Sakuraba Y; Sezutsu H; Takahasi KR; Tsuchihashi K; Ichikawa R; Fujimoto N; Kaneko S; Nakai Y; Uchiyama M; Goda N; Motoi R; Ikeda A; Karashima Y; Inoue M; Kaneda H; Masuya H; Minowa O; Noguchi H; Toyoda A; Sakaki Y; Wakana S; Noda T; Shiroishi T; Gondo Y
Biochem Biophys Res Commun; 2005 Oct; 336(2):609-16. PubMed ID: 16139793
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]