238 related articles for article (PubMed ID: 26819469)
1. FILTUS: a desktop GUI for fast and efficient detection of disease-causing variants, including a novel autozygosity detector.
Vigeland MD; Gjøtterud KS; Selmer KK
Bioinformatics; 2016 May; 32(10):1592-4. PubMed ID: 26819469
[TBL] [Abstract][Full Text] [Related]
2. BCFtools/RoH: a hidden Markov model approach for detecting autozygosity from next-generation sequencing data.
Narasimhan V; Danecek P; Scally A; Xue Y; Tyler-Smith C; Durbin R
Bioinformatics; 2016 Jun; 32(11):1749-51. PubMed ID: 26826718
[TBL] [Abstract][Full Text] [Related]
3. Efficient population-scale variant analysis and prioritization with VAPr.
Birmingham A; Mark AM; Mazzaferro C; Xu G; Fisch KM
Bioinformatics; 2018 Aug; 34(16):2843-2845. PubMed ID: 29659724
[TBL] [Abstract][Full Text] [Related]
4. PhamDB: a web-based application for building Phamerator databases.
Lamine JG; DeJong RJ; Nelesen SM
Bioinformatics; 2016 Jul; 32(13):2026-8. PubMed ID: 27153674
[TBL] [Abstract][Full Text] [Related]
5. PERF: an exhaustive algorithm for ultra-fast and efficient identification of microsatellites from large DNA sequences.
Avvaru AK; Sowpati DT; Mishra RK
Bioinformatics; 2018 Mar; 34(6):943-948. PubMed ID: 29121165
[TBL] [Abstract][Full Text] [Related]
6. MuCor: mutation aggregation and correlation.
Kroll KW; Eisfeld AK; Lozanski G; Bloomfield CD; Byrd JC; Blachly JS
Bioinformatics; 2016 May; 32(10):1557-8. PubMed ID: 26803155
[TBL] [Abstract][Full Text] [Related]
7. PHYLUCE is a software package for the analysis of conserved genomic loci.
Faircloth BC
Bioinformatics; 2016 Mar; 32(5):786-8. PubMed ID: 26530724
[TBL] [Abstract][Full Text] [Related]
8. orfipy: a fast and flexible tool for extracting ORFs.
Singh U; Wurtele ES
Bioinformatics; 2021 Sep; 37(18):3019-3020. PubMed ID: 33576786
[TBL] [Abstract][Full Text] [Related]
9. Jannovar: a java library for exome annotation.
Jäger M; Wang K; Bauer S; Smedley D; Krawitz P; Robinson PN
Hum Mutat; 2014 May; 35(5):548-55. PubMed ID: 24677618
[TBL] [Abstract][Full Text] [Related]
10. Insane in the vembrane: filtering and transforming VCF/BCF files.
Hartmann T; Schröder C; Kuthe E; Lähnemann D; Köster J
Bioinformatics; 2023 Jan; 39(1):. PubMed ID: 36519840
[TBL] [Abstract][Full Text] [Related]
11. HitWalker2: visual analytics for precision medicine and beyond.
Bottomly D; McWeeney SK; Wilmot B
Bioinformatics; 2016 Apr; 32(8):1253-5. PubMed ID: 26708334
[TBL] [Abstract][Full Text] [Related]
12. Bandage: interactive visualization of de novo genome assemblies.
Wick RR; Schultz MB; Zobel J; Holt KE
Bioinformatics; 2015 Oct; 31(20):3350-2. PubMed ID: 26099265
[TBL] [Abstract][Full Text] [Related]
13. JASPAR RESTful API: accessing JASPAR data from any programming language.
Khan A; Mathelier A
Bioinformatics; 2018 May; 34(9):1612-1614. PubMed ID: 29253085
[TBL] [Abstract][Full Text] [Related]
14. CharGer: clinical Characterization of Germline variants.
Scott AD; Huang KL; Weerasinghe A; Mashl RJ; Gao Q; Martins Rodrigues F; Wyczalkowski MA; Ding L
Bioinformatics; 2019 Mar; 35(5):865-867. PubMed ID: 30102335
[TBL] [Abstract][Full Text] [Related]
15. BioBlend: automating pipeline analyses within Galaxy and CloudMan.
Sloggett C; Goonasekera N; Afgan E
Bioinformatics; 2013 Jul; 29(13):1685-6. PubMed ID: 23630176
[TBL] [Abstract][Full Text] [Related]
16. Unified representation of genetic variants.
Tan A; Abecasis GR; Kang HM
Bioinformatics; 2015 Jul; 31(13):2202-4. PubMed ID: 25701572
[TBL] [Abstract][Full Text] [Related]
17. BioNetGen 2.2: advances in rule-based modeling.
Harris LA; Hogg JS; Tapia JJ; Sekar JA; Gupta S; Korsunsky I; Arora A; Barua D; Sheehan RP; Faeder JR
Bioinformatics; 2016 Nov; 32(21):3366-3368. PubMed ID: 27402907
[TBL] [Abstract][Full Text] [Related]
18. Simulated single molecule microscopy with SMeagol.
Lindén M; Ćurić V; Boucharin A; Fange D; Elf J
Bioinformatics; 2016 Aug; 32(15):2394-5. PubMed ID: 27153711
[TBL] [Abstract][Full Text] [Related]
19. GfaPy: a flexible and extensible software library for handling sequence graphs in Python.
Gonnella G; Kurtz S
Bioinformatics; 2017 Oct; 33(19):3094-3095. PubMed ID: 28645150
[TBL] [Abstract][Full Text] [Related]
20. GARLIC: Genomic Autozygosity Regions Likelihood-based Inference and Classification.
Szpiech ZA; Blant A; Pemberton TJ
Bioinformatics; 2017 Jul; 33(13):2059-2062. PubMed ID: 28205676
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]