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Timo Lassmann

Showing results (1-10 of 127) with videos related to

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Nature|February 18, 2026
AI succeeds in diagnosing rare diseasesTimo Lassmann
BMC Bioinformatics|January 29, 2015
TagDust2: a generic method to extract reads from sequencing dataTimo Lassmann
Bioinformatics (Oxford, England)|October 31, 2019
Kalign 3: multiple sequence alignment of large data setsTimo Lassmann
Bioinformatics (Oxford, England)|January 13, 2023
SAMStat 2: quality control for next generation sequencing dataTimo Lassmann
NPJ Genomic Medicine|February 10, 2018
A phenotype centric benchmark of variant prioritisation toolsDenise Anderson, Timo Lassmann
Human Mutation|February 28, 2022
An expanded phenotype centric benchmark of variant prioritisation toolsDenise Anderson, Timo Lassmann
Bioinformatics (Oxford, England)|January 9, 2025
SampleExplorer: using language models to discover relevant transcriptome dataWee Loong Chin, Timo Lassmann
BMC Bioinformatics|July 13, 2007
Automatic extraction of reliable regions from multiple sequence alignmentsTimo Lassmann, Erik Ll Sonnhammer
Nucleic Acids Research|December 20, 2005
Automatic assessment of alignment qualityTimo Lassmann, Erik L L Sonnhammer
Nucleic Acids Research|July 18, 2006
Kalign, Kalignvu and Mumsa: web servers for multiple sequence alignmentTimo Lassmann, Erik L L Sonnhammer
Pageof 13

Showing results (1-10 of 127) with videos related to

Sort By:
Pageof 13
Nature|February 18, 2026
AI succeeds in diagnosing rare diseasesTimo Lassmann
BMC Bioinformatics|January 29, 2015
TagDust2: a generic method to extract reads from sequencing dataTimo Lassmann
Bioinformatics (Oxford, England)|October 31, 2019
Kalign 3: multiple sequence alignment of large data setsTimo Lassmann
Bioinformatics (Oxford, England)|January 13, 2023
SAMStat 2: quality control for next generation sequencing dataTimo Lassmann
NPJ Genomic Medicine|February 10, 2018
A phenotype centric benchmark of variant prioritisation toolsDenise Anderson, Timo Lassmann
Human Mutation|February 28, 2022
An expanded phenotype centric benchmark of variant prioritisation toolsDenise Anderson, Timo Lassmann
Bioinformatics (Oxford, England)|January 9, 2025
SampleExplorer: using language models to discover relevant transcriptome dataWee Loong Chin, Timo Lassmann
BMC Bioinformatics|July 13, 2007
Automatic extraction of reliable regions from multiple sequence alignmentsTimo Lassmann, Erik Ll Sonnhammer
Nucleic Acids Research|December 20, 2005
Automatic assessment of alignment qualityTimo Lassmann, Erik L L Sonnhammer
Nucleic Acids Research|July 18, 2006
Kalign, Kalignvu and Mumsa: web servers for multiple sequence alignmentTimo Lassmann, Erik L L Sonnhammer
Pageof 13