459 related articles for article (PubMed ID: 26210358)
1. VCF-Miner: GUI-based application for mining variants and annotations stored in VCF files.
Hart SN; Duffy P; Quest DJ; Hossain A; Meiners MA; Kocher JP
Brief Bioinform; 2016 Mar; 17(2):346-51. PubMed ID: 26210358
[TBL] [Abstract][Full Text] [Related]
2. VCF-Server: A web-based visualization tool for high-throughput variant data mining and management.
Jiang J; Gu J; Zhao T; Lu H
Mol Genet Genomic Med; 2019 Jul; 7(7):e00641. PubMed ID: 31127704
[TBL] [Abstract][Full Text] [Related]
3. VCF.Filter: interactive prioritization of disease-linked genetic variants from sequencing data.
Müller H; Jimenez-Heredia R; Krolo A; Hirschmugl T; Dmytrus J; Boztug K; Bock C
Nucleic Acids Res; 2017 Jul; 45(W1):W567-W572. PubMed ID: 28520890
[TBL] [Abstract][Full Text] [Related]
4. Variant Call Format-Diagnostic Annotation and Reporting Tool: A Customizable Analysis Pipeline for Identification of Clinically Relevant Genetic Variants in Next-Generation Sequencing Data.
Benton MC; Smith RA; Haupt LM; Sutherland HG; Dunn PJ; Albury CL; Maksemous N; Lea R; Griffiths L
J Mol Diagn; 2019 Nov; 21(6):951-960. PubMed ID: 31442673
[TBL] [Abstract][Full Text] [Related]
5. re-Searcher: GUI-based bioinformatics tool for simplified genomics data mining of VCF files.
Karabayev D; Molkenov A; Yerulanuly K; Kabimoldayev I; Daniyarov A; Sharip A; Seisenova A; Zhumadilov Z; Kairov U
PeerJ; 2021; 9():e11333. PubMed ID: 33987016
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Seshat: A Web service for accurate annotation, validation, and analysis of TP53 variants generated by conventional and next-generation sequencing.
Tikkanen T; Leroy B; Fournier JL; Risques RA; Malcikova J; Soussi T
Hum Mutat; 2018 Jul; 39(7):925-933. PubMed ID: 29696732
[TBL] [Abstract][Full Text] [Related]
8. iVar, an Interpretation-Oriented Tool to Manage the Update and Revision of Variant Annotation and Classification.
Castellano S; Cestari F; Faglioni G; Tenedini E; Marino M; Artuso L; Manfredini R; Luppi M; Trenti T; Tagliafico E
Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33800487
[TBL] [Abstract][Full Text] [Related]
9. DaMold: A data-mining platform for variant annotation and visualization in molecular diagnostics research.
Pandey RV; Pabinger S; Kriegner A; Weinhäusel A
Hum Mutat; 2017 Jul; 38(7):778-787. PubMed ID: 28397319
[TBL] [Abstract][Full Text] [Related]
10. High-Throughput Tabular Data Processor - Platform independent graphical tool for processing large data sets.
Madanecki P; Bałut M; Buckley PG; Ochocka JR; Bartoszewski R; Crossman DK; Messiaen LM; Piotrowski A
PLoS One; 2018; 13(2):e0192858. PubMed ID: 29432475
[TBL] [Abstract][Full Text] [Related]
11. Variant Tool Chest: an improved tool to analyze and manipulate variant call format (VCF) files.
Ebbert MT; Wadsworth ME; Boehme KL; Hoyt KL; Sharp AR; O'Fallon BD; Kauwe JS; Ridge PG
BMC Bioinformatics; 2014; 15 Suppl 7(Suppl 7):S12. PubMed ID: 25080132
[TBL] [Abstract][Full Text] [Related]
12. Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR.
Yang H; Wang K
Nat Protoc; 2015 Oct; 10(10):1556-66. PubMed ID: 26379229
[TBL] [Abstract][Full Text] [Related]
13. 123VCF: an intuitive and efficient tool for filtering VCF files.
Eidi M; Abdolalizadeh S; Moeini S; Garshasbi M; Zahiri J
BMC Bioinformatics; 2024 Feb; 25(1):68. PubMed ID: 38350858
[TBL] [Abstract][Full Text] [Related]
14. WhopGenome: high-speed access to whole-genome variation and sequence data in R.
Wittelsbürger U; Pfeifer B; Lercher MJ
Bioinformatics; 2015 Feb; 31(3):413-5. PubMed ID: 25273104
[TBL] [Abstract][Full Text] [Related]
15. VCF-Explorer: filtering and analysing whole genome VCF files.
Akgün M; Demirci H
Bioinformatics; 2017 Nov; 33(21):3468-3470. PubMed ID: 29036499
[TBL] [Abstract][Full Text] [Related]
16. SNP mining porcine ESTs with MAVIANT, a novel tool for SNP evaluation and annotation.
Panitz F; Stengaard H; Hornshøj H; Gorodkin J; Hedegaard J; Cirera S; Thomsen B; Madsen LB; Høj A; Vingborg RK; Zahn B; Wang X; Wang X; Wernersson R; Jørgensen CB; Scheibye-Knudsen K; Arvin T; Lumholdt S; Sawera M; Green T; Nielsen BJ; Havgaard JH; Brunak S; Fredholm M; Bendixen C
Bioinformatics; 2007 Jul; 23(13):i387-91. PubMed ID: 17646321
[TBL] [Abstract][Full Text] [Related]
17. Gigwa v2-Extended and improved genotype investigator.
Sempéré G; Pétel A; Rouard M; Frouin J; Hueber Y; De Bellis F; Larmande P
Gigascience; 2019 May; 8(5):. PubMed ID: 31077313
[TBL] [Abstract][Full Text] [Related]
18. BrowseVCF: a web-based application and workflow to quickly prioritize disease-causative variants in VCF files.
Salatino S; Ramraj V
Brief Bioinform; 2017 Sep; 18(5):774-779. PubMed ID: 27373737
[TBL] [Abstract][Full Text] [Related]
19. SNVerGUI: a desktop tool for variant analysis of next-generation sequencing data.
Wang W; Hu W; Hou F; Hu P; Wei Z
J Med Genet; 2012 Dec; 49(12):753-5. PubMed ID: 23024288
[TBL] [Abstract][Full Text] [Related]
20. Jointly Integrating VCF-Based Variants and OWL-Based Biomedical Ontologies in MongoDB.
Liu J; Qu Z; Yang M; Sun J; Su S; Zhang L
IEEE/ACM Trans Comput Biol Bioinform; 2020; 17(5):1504-1515. PubMed ID: 31689201
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
