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Nature
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February 18, 2026
AI succeeds in diagnosing rare diseases
Timo Lassmann
BMC Bioinformatics
|
January 29, 2015
TagDust2: a generic method to extract reads from sequencing data
Timo Lassmann
Bioinformatics (Oxford, England)
|
October 31, 2019
Kalign 3: multiple sequence alignment of large data sets
Timo Lassmann
Bioinformatics (Oxford, England)
|
January 13, 2023
SAMStat 2: quality control for next generation sequencing data
Timo Lassmann
NPJ Genomic Medicine
|
February 10, 2018
A phenotype centric benchmark of variant prioritisation tools
Denise Anderson, Timo Lassmann
Human Mutation
|
February 28, 2022
An expanded phenotype centric benchmark of variant prioritisation tools
Denise Anderson, Timo Lassmann
Bioinformatics (Oxford, England)
|
January 9, 2025
SampleExplorer: using language models to discover relevant transcriptome data
Wee Loong Chin, Timo Lassmann
BMC Bioinformatics
|
July 13, 2007
Automatic extraction of reliable regions from multiple sequence alignments
Timo Lassmann, Erik Ll Sonnhammer
Nucleic Acids Research
|
December 20, 2005
Automatic assessment of alignment quality
Timo Lassmann, Erik L L Sonnhammer
Nucleic Acids Research
|
July 18, 2006
Kalign, Kalignvu and Mumsa: web servers for multiple sequence alignment
Timo Lassmann, Erik L L Sonnhammer
Page
of 13
Search research articles
Search
Showing results (1-10 of 127) with videos related to
Sort By:
Page
of 13
Nature
|
February 18, 2026
AI succeeds in diagnosing rare diseases
Timo Lassmann
BMC Bioinformatics
|
January 29, 2015
TagDust2: a generic method to extract reads from sequencing data
Timo Lassmann
Bioinformatics (Oxford, England)
|
October 31, 2019
Kalign 3: multiple sequence alignment of large data sets
Timo Lassmann
Bioinformatics (Oxford, England)
|
January 13, 2023
SAMStat 2: quality control for next generation sequencing data
Timo Lassmann
NPJ Genomic Medicine
|
February 10, 2018
A phenotype centric benchmark of variant prioritisation tools
Denise Anderson, Timo Lassmann
Human Mutation
|
February 28, 2022
An expanded phenotype centric benchmark of variant prioritisation tools
Denise Anderson, Timo Lassmann
Bioinformatics (Oxford, England)
|
January 9, 2025
SampleExplorer: using language models to discover relevant transcriptome data
Wee Loong Chin, Timo Lassmann
BMC Bioinformatics
|
July 13, 2007
Automatic extraction of reliable regions from multiple sequence alignments
Timo Lassmann, Erik Ll Sonnhammer
Nucleic Acids Research
|
December 20, 2005
Automatic assessment of alignment quality
Timo Lassmann, Erik L L Sonnhammer
Nucleic Acids Research
|
July 18, 2006
Kalign, Kalignvu and Mumsa: web servers for multiple sequence alignment
Timo Lassmann, Erik L L Sonnhammer
Page
of 13