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Biorxiv : the Preprint Server for Biology
|
December 11, 2025
Benchmark for simple and complex genome inversions
Siyuan Cheng, Fritz J Sedlazeck
Gigascience
|
July 25, 2020
PhaseME: Automatic rapid assessment of phasing quality and phasing improvement
Sina Majidian, Fritz J Sedlazeck
Nature Reviews. Genetics
|
March 29, 2025
Computational analysis of DNA methylation from long-read sequencing
Yilei Fu, Winston Timp, Fritz J Sedlazeck
Bioinformatics (Oxford, England)
|
August 27, 2013
NextGenMap: fast and accurate read mapping in highly polymorphic genomes
Fritz J Sedlazeck, Philipp Rescheneder, Arndt von Haeseler
Genome Research
|
April 14, 2025
A Hitchhiker's Guide to long-read genomic analysis
Medhat Mahmoud, Daniel P Agustinho, Fritz J Sedlazeck
Gigascience
|
September 9, 2019
Evaluation of computational genotyping of structural variation for clinical diagnoses
Varuna Chander, Richard A Gibbs, Fritz J Sedlazeck
Biorxiv : the Preprint Server for Biology
|
February 9, 2026
A systematic assessment of machine learning for structural variant filtering
Archit Kalra, Luis F Paulin, Fritz J Sedlazeck
Nature Reviews. Genetics
|
May 29, 2021
Towards population-scale long-read sequencing
Wouter De Coster, Matthias H Weissensteiner, Fritz J Sedlazeck
Genome Biology
|
September 15, 2021
PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation
Medhat Mahmoud, Harshavardhan Doddapaneni, Winston Timp, et al.
Nature Protocols
|
June 8, 2026
Structural variant calling using Sniffles2
Luis F Paulin, Hermann Romanek, Farhang Jaryani, et al.
Page
of 20
Search research articles
Search
Showing results (1-10 of 196) with videos related to
Sort By:
Page
of 20
Biorxiv : the Preprint Server for Biology
|
December 11, 2025
Benchmark for simple and complex genome inversions
Siyuan Cheng, Fritz J Sedlazeck
Gigascience
|
July 25, 2020
PhaseME: Automatic rapid assessment of phasing quality and phasing improvement
Sina Majidian, Fritz J Sedlazeck
Nature Reviews. Genetics
|
March 29, 2025
Computational analysis of DNA methylation from long-read sequencing
Yilei Fu, Winston Timp, Fritz J Sedlazeck
Bioinformatics (Oxford, England)
|
August 27, 2013
NextGenMap: fast and accurate read mapping in highly polymorphic genomes
Fritz J Sedlazeck, Philipp Rescheneder, Arndt von Haeseler
Genome Research
|
April 14, 2025
A Hitchhiker's Guide to long-read genomic analysis
Medhat Mahmoud, Daniel P Agustinho, Fritz J Sedlazeck
Gigascience
|
September 9, 2019
Evaluation of computational genotyping of structural variation for clinical diagnoses
Varuna Chander, Richard A Gibbs, Fritz J Sedlazeck
Biorxiv : the Preprint Server for Biology
|
February 9, 2026
A systematic assessment of machine learning for structural variant filtering
Archit Kalra, Luis F Paulin, Fritz J Sedlazeck
Nature Reviews. Genetics
|
May 29, 2021
Towards population-scale long-read sequencing
Wouter De Coster, Matthias H Weissensteiner, Fritz J Sedlazeck
Genome Biology
|
September 15, 2021
PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation
Medhat Mahmoud, Harshavardhan Doddapaneni, Winston Timp, et al.
Nature Protocols
|
June 8, 2026
Structural variant calling using Sniffles2
Luis F Paulin, Hermann Romanek, Farhang Jaryani, et al.
Page
of 20