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 *

184 related articles for article (PubMed ID: 37312221)

  • 21. Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities.
    Falk MJ; Shen L; Gonzalez M; Leipzig J; Lott MT; Stassen AP; Diroma MA; Navarro-Gomez D; Yeske P; Bai R; Boles RG; Brilhante V; Ralph D; DaRe JT; Shelton R; Terry SF; Zhang Z; Copeland WC; van Oven M; Prokisch H; Wallace DC; Attimonelli M; Krotoski D; Zuchner S; Gai X; ; ; ; ; ;
    Mol Genet Metab; 2015 Mar; 114(3):388-96. PubMed ID: 25542617
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Novel gene variants in patients with platelet-based bleeding using combined exome sequencing and RNAseq murine expression data.
    Khan AO; Stapley RJ; Pike JA; Wijesinghe SN; Reyat JS; Almazni I; Machlus KR; Morgan NV;
    J Thromb Haemost; 2021 Jan; 19(1):262-268. PubMed ID: 33021027
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Whole exome sequencing (WES) on formalin-fixed, paraffin-embedded (FFPE) tumor tissue in gastrointestinal stromal tumors (GIST).
    Astolfi A; Urbini M; Indio V; Nannini M; Genovese CG; Santini D; Saponara M; Mandrioli A; Ercolani G; Brandi G; Biasco G; Pantaleo MA
    BMC Genomics; 2015 Nov; 16():892. PubMed ID: 26531060
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2.
    D'Aurizio R; Pippucci T; Tattini L; Giusti B; Pellegrini M; Magi A
    Nucleic Acids Res; 2016 Nov; 44(20):e154. PubMed ID: 27507884
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
    Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
    Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prioritization of oligogenic variant combinations in whole exomes.
    Gravel B; Renaux A; Papadimitriou S; Smits G; Nowé A; Lenaerts T
    Bioinformatics; 2024 Mar; 40(4):. PubMed ID: 38603604
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Replicate exome-sequencing in a multiple-generation family: improved interpretation of next-generation sequencing data.
    Cherukuri PF; Maduro V; Fuentes-Fajardo KV; Lam K; ; Adams DR; Tifft CJ; Mullikin JC; Gahl WA; Boerkoel CF
    BMC Genomics; 2015 Nov; 16():998. PubMed ID: 26602380
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdb.
    Tan PP; Rogic S; Zoubarev A; McDonald C; Lui F; Charathsandran G; Jacobson M; Belmadani M; Leong J; Van Rossum T; Portales-Casamar E; Qiao Y; Calli K; Liu X; Hudson M; Rajcan-Separovic E; Lewis MS; Pavlidis P
    Hum Mutat; 2016 Aug; 37(8):719-26. PubMed ID: 27158917
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder.
    Kim N; Kim KH; Lim WJ; Kim J; Kim SA; Yoo HJ
    Genes (Basel); 2020 Dec; 12(1):. PubMed ID: 33374967
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification of potential causal variants for premature ovarian failure by whole exome sequencing.
    Jin H; Ahn J; Park Y; Sim J; Park HS; Ryu CS; Kim NK; Kwack K
    BMC Med Genomics; 2020 Oct; 13(1):159. PubMed ID: 33109206
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate.
    Charng WL; Karaca E; Coban Akdemir Z; Gambin T; Atik MM; Gu S; Posey JE; Jhangiani SN; Muzny DM; Doddapaneni H; Hu J; Boerwinkle E; Gibbs RA; Rosenfeld JA; Cui H; Xia F; Manickam K; Yang Y; Faqeih EA; Al Asmari A; Saleh MA; El-Hattab AW; Lupski JR
    BMC Med Genomics; 2016 Jul; 9(1):42. PubMed ID: 27435318
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Increase in diagnostic yield achieved for 174 whole-exome sequencing cases reanalyzed 1-2 years after initial analysis.
    Liu Y; Teng Y; Li Z; Cui J; Liang D; Wu L
    Clin Chim Acta; 2021 Dec; 523():163-168. PubMed ID: 34560057
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Var2GO: a web-based tool for gene variants selection.
    Granata I; Sangiovanni M; Maiorano F; Miele M; Guarracino MR
    BMC Bioinformatics; 2016 Nov; 17(Suppl 12):376. PubMed ID: 28185576
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES).
    Liu Y; Cao Y; Li Y; Lei D; Li L; Hou ZL; Han S; Meng M; Shi J; Zhang Y; Wang Y; Niu Z; Xie Y; Xiao B; Wang Y; Li X; Yang L; Wang W; Jiang L
    Med Sci Monit; 2018 Mar; 24():1340-1358. PubMed ID: 29505555
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Whole exome sequencing in molecular diagnostics of cancer decreases over time: evidence from a cost analysis in the French setting.
    Bayle A; Droin N; Besse B; Zou Z; Boursin Y; Rissel S; Solary E; Lacroix L; Rouleau E; Borget I; Bonastre J
    Eur J Health Econ; 2021 Aug; 22(6):855-864. PubMed ID: 33765190
    [TBL] [Abstract][Full Text] [Related]  

  • 36. DIscBIO: A User-Friendly Pipeline for Biomarker Discovery in Single-Cell Transcriptomics.
    Ghannoum S; Leoncio Netto W; Fantini D; Ragan-Kelley B; Parizadeh A; Jonasson E; Ståhlberg A; Farhan H; Köhn-Luque A
    Int J Mol Sci; 2021 Jan; 22(3):. PubMed ID: 33573289
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Protocol for unbiased, consolidated variant calling from whole exome sequencing data.
    Verrou KM; Pavlopoulos GA; Moulos P
    STAR Protoc; 2022 Jun; 3(2):101418. PubMed ID: 35669050
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.
    Belkadi A; Bolze A; Itan Y; Cobat A; Vincent QB; Antipenko A; Shang L; Boisson B; Casanova JL; Abel L
    Proc Natl Acad Sci U S A; 2015 Apr; 112(17):5473-8. PubMed ID: 25827230
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Implementation of whole-exome sequencing for pharmacogenomics profiling and exploring its potential clinical utilities.
    Wang D; Bolleddula J; Coenen-Stass A; Grombacher T; Dong JQ; Scheuenpflug J; Locatelli G; Feng Z
    Pharmacogenomics; 2024 Mar; 25(4):197-206. PubMed ID: 38511470
    [TBL] [Abstract][Full Text] [Related]  

  • 40. ERDS-exome: a Hybrid Approach for Copy Number Variant Detection from Whole-exome Sequencing Data.
    Tan R; Wang J; Wu X; Juan L; Zheng L; Ma R; Zhan Q; Wang T; Jin S; Jiang Q; Wang Y
    IEEE/ACM Trans Comput Biol Bioinform; 2017 Oct; ():. PubMed ID: 28981421
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.