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.
5289 related articles for article (PubMed ID: 19346325)
1. DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Librado P; Rozas J Bioinformatics; 2009 Jun; 25(11):1451-2. PubMed ID: 19346325 [TBL] [Abstract][Full Text] [Related]
2. DnaSP, DNA polymorphism analyses by the coalescent and other methods. Rozas J; Sánchez-DelBarrio JC; Messeguer X; Rozas R Bioinformatics; 2003 Dec; 19(18):2496-7. PubMed ID: 14668244 [TBL] [Abstract][Full Text] [Related]
3. DnaSP 6: DNA Sequence Polymorphism Analysis of Large Data Sets. Rozas J; Ferrer-Mata A; Sánchez-DelBarrio JC; Guirao-Rico S; Librado P; Ramos-Onsins SE; Sánchez-Gracia A Mol Biol Evol; 2017 Dec; 34(12):3299-3302. PubMed ID: 29029172 [TBL] [Abstract][Full Text] [Related]
4. DnaSP version 3: an integrated program for molecular population genetics and molecular evolution analysis. Rozas J; Rozas R Bioinformatics; 1999 Feb; 15(2):174-5. PubMed ID: 10089204 [TBL] [Abstract][Full Text] [Related]
6. DnaSP version 2.0: a novel software package for extensive molecular population genetics analysis. Rozas J; Rozas R Comput Appl Biosci; 1997 Jun; 13(3):307-11. PubMed ID: 9183537 [TBL] [Abstract][Full Text] [Related]
7. RNASeqBrowser: a genome browser for simultaneous visualization of raw strand specific RNAseq reads and UCSC genome browser custom tracks. An J; Lai J; Wood DL; Sajjanhar A; Wang C; Tevz G; Lehman ML; Nelson CC BMC Genomics; 2015 Mar; 16(1):145. PubMed ID: 25766521 [TBL] [Abstract][Full Text] [Related]
8. BigWig and BigBed: enabling browsing of large distributed datasets. Kent WJ; Zweig AS; Barber G; Hinrichs AS; Karolchik D Bioinformatics; 2010 Sep; 26(17):2204-7. PubMed ID: 20639541 [TBL] [Abstract][Full Text] [Related]
9. HAPLOWSER: a whole-genome haplotype browser for personal genome and metagenome. Kim JH; Kim WC; Waterman MS; Park S; Li LM Bioinformatics; 2009 Sep; 25(18):2430-1. PubMed ID: 19561337 [TBL] [Abstract][Full Text] [Related]
11. DIYABC v2.0: a software to make approximate Bayesian computation inferences about population history using single nucleotide polymorphism, DNA sequence and microsatellite data. Cornuet JM; Pudlo P; Veyssier J; Dehne-Garcia A; Gautier M; Leblois R; Marin JM; Estoup A Bioinformatics; 2014 Apr; 30(8):1187-1189. PubMed ID: 24389659 [TBL] [Abstract][Full Text] [Related]
13. A method for identifying haplotypes carrying the causative allele in positive natural selection and genome-wide association studies. Ong RT; Liu X; Poh WT; Sim X; Chia KS; Teo YY Bioinformatics; 2011 Mar; 27(6):822-8. PubMed ID: 21216773 [TBL] [Abstract][Full Text] [Related]
14. Processing and population genetic analysis of multigenic datasets with ProSeq3 software. Filatov DA Bioinformatics; 2009 Dec; 25(23):3189-90. PubMed ID: 19797407 [TBL] [Abstract][Full Text] [Related]
15. WebGBrowse--a web server for GBrowse. Podicheti R; Gollapudi R; Dong Q Bioinformatics; 2009 Jun; 25(12):1550-1. PubMed ID: 19357095 [TBL] [Abstract][Full Text] [Related]
18. Visualizing Genomic Annotations with the UCSC Genome Browser. Hung JH; Weng Z Cold Spring Harb Protoc; 2016 Nov; 2016(11):. PubMed ID: 27574198 [TBL] [Abstract][Full Text] [Related]
19. HapSim: a simulation tool for generating haplotype data with pre-specified allele frequencies and LD coefficients. Montana G Bioinformatics; 2005 Dec; 21(23):4309-11. PubMed ID: 16188927 [TBL] [Abstract][Full Text] [Related]