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Genome Medicine
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October 8, 2024
Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR
Stephan Amstler, Gertraud Streiter, Cathrin Pfurtscheller, et al.
NAR Genomics and Bioinformatics
|
February 8, 2024
Performing highly parallelized and reproducible GWAS analysis on biobank-scale data
Sebastian Schönherr, Johanna F Schachtl-Riess, Silvia Di Maio, et al.
American Journal of Human Genetics
|
May 4, 2022
Meta-imputation: An efficient method to combine genotype data after imputation with multiple reference panels
Ketian Yu, Sayantan Das, Jonathon LeFaive, et al.
International Journal of Molecular Sciences
|
January 22, 2021
Analyzing Low-Level mtDNA Heteroplasmy-Pitfalls and Challenges from Bench to Benchmarking
Federica Fazzini, Liane Fendt, Sebastian Schönherr, et al.
BMC Bioinformatics
|
June 16, 2010
CONAN: copy number variation analysis software for genome-wide association studies
Lukas Forer, Sebastian Schönherr, Hansi Weissensteiner, et al.
Nucleic Acids Research
|
May 6, 2024
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers
Lukas Forer, Daniel Taliun, Jonathon LeFaive, et al.
Journal of Lipid Research
|
October 29, 2022
The kringle IV type 2 domain variant 4925G>A causes the elusive association signal of the LPA pentanucleotide repeat
Rebecca Grüneis, Hansi Weissensteiner, Claudia Lamina, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
April 7, 2022
PCSK9 and Cardiovascular Disease in Individuals with Moderately Decreased Kidney Function
Azin Kheirkhah, Claudia Lamina, Barbara Kollerits, et al.
British Journal of Anaesthesia
|
May 4, 2021
Complex regional pain syndrome: role of contralateral sensitisation
Christopher Dietz, Ann-Kristin Reinhold, Fabiola Escolano-Lozano, et al.
Nucleic Acids Research
|
May 16, 2025
CRISPR-BEasy: a free web-based service for designing sgRNA tiling libraries for CRISPR-dependent base editing screens
Vincent Chapdelaine-Trépanier, Shamika Shenoy, Wardah Masud, et al.
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of 9
Search research articles
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Showing results (21-30 of 87) with videos related to
Sort By:
Page
of 9
Genome Medicine
|
October 8, 2024
Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR
Stephan Amstler, Gertraud Streiter, Cathrin Pfurtscheller, et al.
NAR Genomics and Bioinformatics
|
February 8, 2024
Performing highly parallelized and reproducible GWAS analysis on biobank-scale data
Sebastian Schönherr, Johanna F Schachtl-Riess, Silvia Di Maio, et al.
American Journal of Human Genetics
|
May 4, 2022
Meta-imputation: An efficient method to combine genotype data after imputation with multiple reference panels
Ketian Yu, Sayantan Das, Jonathon LeFaive, et al.
International Journal of Molecular Sciences
|
January 22, 2021
Analyzing Low-Level mtDNA Heteroplasmy-Pitfalls and Challenges from Bench to Benchmarking
Federica Fazzini, Liane Fendt, Sebastian Schönherr, et al.
BMC Bioinformatics
|
June 16, 2010
CONAN: copy number variation analysis software for genome-wide association studies
Lukas Forer, Sebastian Schönherr, Hansi Weissensteiner, et al.
Nucleic Acids Research
|
May 6, 2024
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers
Lukas Forer, Daniel Taliun, Jonathon LeFaive, et al.
Journal of Lipid Research
|
October 29, 2022
The kringle IV type 2 domain variant 4925G>A causes the elusive association signal of the LPA pentanucleotide repeat
Rebecca Grüneis, Hansi Weissensteiner, Claudia Lamina, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
April 7, 2022
PCSK9 and Cardiovascular Disease in Individuals with Moderately Decreased Kidney Function
Azin Kheirkhah, Claudia Lamina, Barbara Kollerits, et al.
British Journal of Anaesthesia
|
May 4, 2021
Complex regional pain syndrome: role of contralateral sensitisation
Christopher Dietz, Ann-Kristin Reinhold, Fabiola Escolano-Lozano, et al.
Nucleic Acids Research
|
May 16, 2025
CRISPR-BEasy: a free web-based service for designing sgRNA tiling libraries for CRISPR-dependent base editing screens
Vincent Chapdelaine-Trépanier, Shamika Shenoy, Wardah Masud, et al.
Page
of 9