386 related articles for article (PubMed ID: 25139187)
1. Using next-generation sequencing to isolate mutant genes from forward genetic screens.
Schneeberger K
Nat Rev Genet; 2014 Oct; 15(10):662-76. PubMed ID: 25139187
[TBL] [Abstract][Full Text] [Related]
2. Genetic screens for mutations affecting adult traits and parental-effect genes.
Pelegri F; Mullins MC
Methods Cell Biol; 2016; 135():39-87. PubMed ID: 27443920
[TBL] [Abstract][Full Text] [Related]
3. Identification of EMS-induced causal mutations in a non-reference Arabidopsis thaliana accession by whole genome sequencing.
Uchida N; Sakamoto T; Kurata T; Tasaka M
Plant Cell Physiol; 2011 Apr; 52(4):716-22. PubMed ID: 21398646
[TBL] [Abstract][Full Text] [Related]
4. MutMap+: genetic mapping and mutant identification without crossing in rice.
Fekih R; Takagi H; Tamiru M; Abe A; Natsume S; Yaegashi H; Sharma S; Sharma S; Kanzaki H; Matsumura H; Saitoh H; Mitsuoka C; Utsushi H; Uemura A; Kanzaki E; Kosugi S; Yoshida K; Cano L; Kamoun S; Terauchi R
PLoS One; 2013; 8(7):e68529. PubMed ID: 23874658
[TBL] [Abstract][Full Text] [Related]
5. RNA-seq-based mapping and candidate identification of mutations from forward genetic screens.
Miller AC; Obholzer ND; Shah AN; Megason SG; Moens CB
Genome Res; 2013 Apr; 23(4):679-86. PubMed ID: 23299976
[TBL] [Abstract][Full Text] [Related]
6. Mutation Mapping and Identification by Whole-Genome Sequencing.
Smith HE
Methods Mol Biol; 2022; 2468():257-269. PubMed ID: 35320569
[TBL] [Abstract][Full Text] [Related]
7. SHOREmap v3.0: fast and accurate identification of causal mutations from forward genetic screens.
Sun H; Schneeberger K
Methods Mol Biol; 2015; 1284():381-95. PubMed ID: 25757783
[TBL] [Abstract][Full Text] [Related]
8. Mapping-by-Sequencing of Point and Insertional Mutations with Easymap.
Lup SD; Wilson-Sánchez D; Micol JL
Methods Mol Biol; 2022; 2484():343-361. PubMed ID: 35461462
[TBL] [Abstract][Full Text] [Related]
9. The application of MutMap in forward genetic studies based on whole-genome sequencing.
Yuan JH; Li JH; Yuan JJ; Jia KL; Li SF; Deng CL; Gao WJ
Yi Chuan; 2017 Dec; 39(12):1168-1177. PubMed ID: 29258987
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Molecular genetic analysis of PKHD1 by next-generation sequencing in Czech families with autosomal recessive polycystic kidney disease.
Obeidova L; Seeman T; Elisakova V; Reiterova J; Puchmajerova A; Stekrova J
BMC Med Genet; 2015 Dec; 16():116. PubMed ID: 26695994
[TBL] [Abstract][Full Text] [Related]
12. Common neurodegenerative diseases: dissection by genome-wide association.
Bonifati V
Curr Neurol Neurosci Rep; 2007 Sep; 7(5):425-7. PubMed ID: 17764633
[TBL] [Abstract][Full Text] [Related]
13. Next-generation forward genetic screens: using simulated data to improve the design of mapping-by-sequencing experiments in Arabidopsis.
Wilson-Sánchez D; Lup SD; Sarmiento-Mañús R; Ponce MR; Micol JL
Nucleic Acids Res; 2019 Dec; 47(21):e140. PubMed ID: 31544937
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Identification of mutations in zebrafish using next-generation sequencing.
Henke K; Bowen ME; Harris MP
Curr Protoc Mol Biol; 2013 Oct; 104():7.13.1-7.13.33. PubMed ID: 24510885
[TBL] [Abstract][Full Text] [Related]
16. Next-Gen Sequencing-Based Mapping and Identification of Ethyl Methanesulfonate-Induced Mutations in Arabidopsis thaliana.
Zhang XC; Millet Y; Ausubel FM; Borowsky M
Curr Protoc Mol Biol; 2014 Oct; 108():7.18.1-7.18.16. PubMed ID: 25271717
[TBL] [Abstract][Full Text] [Related]
17. Use of linkage analysis, genome-wide association studies, and next-generation sequencing in the identification of disease-causing mutations.
Londin E; Yadav P; Surrey S; Kricka LJ; Fortina P
Methods Mol Biol; 2013; 1015():127-46. PubMed ID: 23824853
[TBL] [Abstract][Full Text] [Related]
18. The genetic basis for psychiatric illness in man.
Tandon K; McGuffin P
Eur J Neurosci; 2002 Aug; 16(3):403-7. PubMed ID: 12193182
[TBL] [Abstract][Full Text] [Related]
19. Mapping Maize Mutants Using Bulked-Segregant Analysis and Next-Generation Sequencing.
Best NB; McSteen P
Curr Protoc; 2022 Nov; 2(11):e591. PubMed ID: 36350247
[TBL] [Abstract][Full Text] [Related]
20. Synteny-based mapping-by-sequencing enabled by targeted enrichment.
Galvão VC; Nordström KJ; Lanz C; Sulz P; Mathieu J; Posé D; Schmid M; Weigel D; Schneeberger K
Plant J; 2012 Aug; 71(3):517-26. PubMed ID: 22409706
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]