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Biorxiv : the Preprint Server for Biology
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February 9, 2026
A systematic assessment of machine learning for structural variant filtering
Archit Kalra, Luis F Paulin, Fritz J Sedlazeck
Nature Protocols
|
June 8, 2026
Structural variant calling using Sniffles2
Luis F Paulin, Hermann Romanek, Farhang Jaryani, et al.
Acta Neuropathologica Communications
|
August 21, 2025
Germline structural variations involving the pediatric brain tumor transcriptome include disease-relevant and ancestry-related genes
Fengju Chen, Yiqun Zhang, Luis F Paulin, et al.
BMC Bioinformatics
|
January 20, 2023
SVhound: detection of regions that harbor yet undetected structural variation
Luis F Paulin, Muthuswamy Raveendran, R Alan Harris, et al.
Nature Methods
|
November 30, 2023
Improved sequence mapping using a complete reference genome and lift-over
Nae-Chyun Chen, Luis F Paulin, Fritz J Sedlazeck, et al.
Nature Communications
|
April 14, 2026
Global impact of germline structural variation on the cancer proteome
Fengju Chen, Yiqun Zhang, Luis F Paulin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 2, 2024
The benefit of a complete reference genome for cancer structural variant analysis
Luis F Paulin, Jeremy Fan, Kieran O'Neill, et al.
Genome Research
|
March 17, 2025
Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T
Luis F Paulin, Jeremy Fan, Kieran O'Neill, et al.
Nature Communications
|
September 26, 2020
Poly(ADP-ribose) glycohydrolase coordinates meiotic DNA double-strand break induction and repair independent of its catalytic activity
Eva Janisiw, Marilina Raices, Fabiola Balmir, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 27, 2026
Comprehensive detection of genetic and epigenetic alterations in cancer using long reads with TumorLens
Luis F Paulin, Minyi Shi, Yilei Fu, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 29) with videos related to
Sort By:
Page
of 3
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 Protocols
|
June 8, 2026
Structural variant calling using Sniffles2
Luis F Paulin, Hermann Romanek, Farhang Jaryani, et al.
Acta Neuropathologica Communications
|
August 21, 2025
Germline structural variations involving the pediatric brain tumor transcriptome include disease-relevant and ancestry-related genes
Fengju Chen, Yiqun Zhang, Luis F Paulin, et al.
BMC Bioinformatics
|
January 20, 2023
SVhound: detection of regions that harbor yet undetected structural variation
Luis F Paulin, Muthuswamy Raveendran, R Alan Harris, et al.
Nature Methods
|
November 30, 2023
Improved sequence mapping using a complete reference genome and lift-over
Nae-Chyun Chen, Luis F Paulin, Fritz J Sedlazeck, et al.
Nature Communications
|
April 14, 2026
Global impact of germline structural variation on the cancer proteome
Fengju Chen, Yiqun Zhang, Luis F Paulin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 2, 2024
The benefit of a complete reference genome for cancer structural variant analysis
Luis F Paulin, Jeremy Fan, Kieran O'Neill, et al.
Genome Research
|
March 17, 2025
Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T
Luis F Paulin, Jeremy Fan, Kieran O'Neill, et al.
Nature Communications
|
September 26, 2020
Poly(ADP-ribose) glycohydrolase coordinates meiotic DNA double-strand break induction and repair independent of its catalytic activity
Eva Janisiw, Marilina Raices, Fabiola Balmir, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 27, 2026
Comprehensive detection of genetic and epigenetic alterations in cancer using long reads with TumorLens
Luis F Paulin, Minyi Shi, Yilei Fu, et al.
Page
of 3