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NPJ Genomic Medicine|February 10, 2018
A phenotype centric benchmark of variant prioritisation toolsDenise Anderson, Timo LassmannHuman Mutation|February 28, 2022
An expanded phenotype centric benchmark of variant prioritisation toolsDenise Anderson, Timo LassmannNature Communications|November 23, 2019
Personalised analytics for rare disease diagnosticsDenise Anderson, Gareth Baynam, Jenefer M Blackwell, et al.BMC Bioinformatics|January 29, 2015
TagDust2: a generic method to extract reads from sequencing dataTimo LassmannBioinformatics (Oxford, England)|October 31, 2019
Kalign 3: multiple sequence alignment of large data setsTimo LassmannBioinformatics (Oxford, England)|January 13, 2023
SAMStat 2: quality control for next generation sequencing dataTimo LassmannScientific Data|April 13, 2016
Reference genotype and exome data from an Australian Aboriginal population for health-based researchDave Tang, Denise Anderson, Richard W Francis, et al.Bioinformatics (Oxford, England)|January 9, 2025
SampleExplorer: using language models to discover relevant transcriptome dataWee Loong Chin, Timo LassmannBMC Bioinformatics|July 13, 2007
Automatic extraction of reliable regions from multiple sequence alignmentsTimo Lassmann, Erik Ll SonnhammerNucleic Acids Research|December 20, 2005
Automatic assessment of alignment qualityTimo Lassmann, Erik L L SonnhammerPageof 17