These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 23171430)

  • 1. Exon capture and bulk segregant analysis: rapid discovery of causative mutations using high-throughput sequencing.
    del Viso F; Bhattacharya D; Kong Y; Gilchrist MJ; Khokha MK
    BMC Genomics; 2012 Nov; 13():649. PubMed ID: 23171430
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic analysis of Xenopus tropicalis.
    Geach TJ; Stemple DL; Zimmerman LB
    Methods Mol Biol; 2012; 917():69-110. PubMed ID: 22956083
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome-wide DNA capture and next generation sequencing in domestic and wild species.
    Cosart T; Beja-Pereira A; Chen S; Ng SB; Shendure J; Luikart G
    BMC Genomics; 2011 Jul; 12():347. PubMed ID: 21729323
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mapping causal mutations by exome sequencing in a wheat TILLING population: a tall mutant case study.
    Mo Y; Howell T; Vasquez-Gross H; de Haro LA; Dubcovsky J; Pearce S
    Mol Genet Genomics; 2018 Apr; 293(2):463-477. PubMed ID: 29188438
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Exome capture sequencing identifies a novel mutation in BBS4.
    Wang H; Chen X; Dudinsky L; Patenia C; Chen Y; Li Y; Wei Y; Abboud EB; Al-Rajhi AA; Lewis RA; Lupski JR; Mardon G; Gibbs RA; Perkins BD; Chen R
    Mol Vis; 2011; 17():3529-40. PubMed ID: 22219648
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rapid fine mapping of causative mutations from sets of unordered, contig-sized fragments of genome sequence.
    Rallapalli G; Corredor-Moreno P; Chalstrey E; Page M; MacLean D
    BMC Bioinformatics; 2019 Jan; 20(1):9. PubMed ID: 30616525
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models.
    Andrews TD; Whittle B; Field MA; Balakishnan B; Zhang Y; Shao Y; Cho V; Kirk M; Singh M; Xia Y; Hager J; Winslade S; Sjollema G; Beutler B; Enders A; Goodnow CC
    Open Biol; 2012 May; 2(5):120061. PubMed ID: 22724066
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deletion Mutagenesis and Identification of Causative Mutations in Maize.
    Jia S; Li A; Zhang C; Holding D
    Methods Mol Biol; 2018; 1676():97-108. PubMed ID: 28986905
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Discovery of pod shatter-resistant associated SNPs by deep sequencing of a representative library followed by bulk segregant analysis in rapeseed.
    Hu Z; Hua W; Huang S; Yang H; Zhan G; Wang X; Liu G; Wang H
    PLoS One; 2012; 7(4):e34253. PubMed ID: 22529909
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A genetic map of Xenopus tropicalis.
    Wells DE; Gutierrez L; Xu Z; Krylov V; Macha J; Blankenburg KP; Hitchens M; Bellot LJ; Spivey M; Stemple DL; Kowis A; Ye Y; Pasternak S; Owen J; Tran T; Slavikova R; Tumova L; Tlapakova T; Seifertova E; Scherer SE; Sater AK
    Dev Biol; 2011 Jun; 354(1):1-8. PubMed ID: 21458440
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bulk segregant analysis followed by high-throughput sequencing reveals the Neurospora cell cycle gene, ndc-1, to be allelic with the gene for ornithine decarboxylase, spe-1.
    Pomraning KR; Smith KM; Freitag M
    Eukaryot Cell; 2011 Jun; 10(6):724-33. PubMed ID: 21515825
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Comparison of SureSelect and Nextera Exome Capture Performance in Single-Cell Sequencing.
    Huss WJ; Hu Q; Glenn ST; Gangavarapu KJ; Wang J; Luce JD; Quinn PK; Brese EA; Zhan F; Conroy JM; Paragh G; Foster BA; Morrison CD; Liu S; Wei L
    Hum Hered; 2018; 83(3):153-162. PubMed ID: 30669152
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Nucleotide polymorphism and copy number variant detection using exome capture and next-generation sequencing in the polyploid grass Panicum virgatum.
    Evans J; Kim J; Childs KL; Vaillancourt B; Crisovan E; Nandety A; Gerhardt DJ; Richmond TA; Jeddeloh JA; Kaeppler SM; Casler MD; Buell CR
    Plant J; 2014 Sep; 79(6):993-1008. PubMed ID: 24947485
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rapid gynogenetic mapping of Xenopus tropicalis mutations to chromosomes.
    Khokha MK; Krylov V; Reilly MJ; Gall JG; Bhattacharya D; Cheung CY; Kaufman S; Lam DK; Macha J; Ngo C; Prakash N; Schmidt P; Tlapakova T; Trivedi T; Tumova L; Abu-Daya A; Geach T; Vendrell E; Ironfield H; Sinzelle L; Sater AK; Wells DE; Harland RM; Zimmerman LB
    Dev Dyn; 2009 Jun; 238(6):1398-46. PubMed ID: 19441086
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A high-density gene map of loblolly pine (Pinus taeda L.) based on exome sequence capture genotyping.
    Neves LG; Davis JM; Barbazuk WB; Kirst M
    G3 (Bethesda); 2014 Jan; 4(1):29-37. PubMed ID: 24192835
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement.
    Bowne SJ; Humphries MM; Sullivan LS; Kenna PF; Tam LC; Kiang AS; Campbell M; Weinstock GM; Koboldt DC; Ding L; Fulton RS; Sodergren EJ; Allman D; Millington-Ward S; Palfi A; McKee A; Blanton SH; Slifer S; Konidari I; Farrar GJ; Daiger SP; Humphries P
    Eur J Hum Genet; 2011 Oct; 19(10):1074-81. PubMed ID: 21654732
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.