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Genome Biology|December 25, 2012
cnvHiTSeq: integrative models for high-resolution copy number variation detection and genotyping using population sequencing dataEvangelos Bellos, Michael R Johnson, Lachlan J M CoinBioinformatics (Oxford, England)|August 28, 2014
cnvOffSeq: detecting intergenic copy number variation using off-target exome sequencing dataEvangelos Bellos, Lachlan J M CoinGenome Biology|October 30, 2012
Bioinformatics: living on the edgeEvangelos Bellos, Lachlan J M Coin, Myrsini KaforouNucleic Acids Research|December 11, 2012
A population model for genotyping indels from next-generation sequence dataHaojing Shao, Evangelos Bellos, Hanjiudai Yin, et al.Gigascience|April 4, 2024
Pangenome databases improve host removal and mycobacteria classification from clinical metagenomic dataMichael B Hall, Lachlan J M CoinNucleic Acids Research|September 18, 2014
cnvCapSeq: detecting copy number variation in long-range targeted resequencing dataEvangelos Bellos, Vikrant Kumar, Clarabelle Lin, et al.Bioinformatics (Oxford, England)|November 9, 2025
Genome size estimation from long read overlapsMichael B Hall, Chenxi Zhou, Lachlan J M CoinPlos Computational Biology|January 20, 2021
Real-time resolution of short-read assembly graph using ONT long readsSon Hoang Nguyen, Minh Duc Cao, Lachlan J M CoinBioinformatics (Oxford, England)|January 29, 2010
invertFREGENE: software for simulating inversions in population genetic dataPaul F O'Reilly, Lachlan J M Coin, Clive J HoggartBioinformatics (Oxford, England)|February 26, 2008
Disease association tests by inferring ancestral haplotypes using a hidden markov modelShu-Yi Su, David J Balding, Lachlan J M CoinPageof 20