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Martin Kircher

Showing results (11-20 of 89) with videos related to

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Gigascience|April 21, 2023
The Regulatory Mendelian Mutation score for GRCh38Max Schubach, Lusiné Nazaretyan, Martin Kircher
Nucleic Acids Research|October 25, 2011
Double indexing overcomes inaccuracies in multiplex sequencing on the Illumina platformMartin Kircher, Susanna Sawyer, Matthias Meyer
Plos Computational Biology|June 5, 2020
HemoMIPs-Automated analysis and result reporting pipeline for targeted sequencing dataPhilip Kleinert, Beth Martin, Martin Kircher
Genome Medicine|August 4, 2025
varCADD: large sets of standing genetic variation enable genome-wide pathogenicity predictionLusiné Nazaretyan, Philipp Rentzsch, Martin Kircher
BMC Genomics|August 2, 2011
Addressing challenges in the production and analysis of illumina sequencing dataMartin Kircher, Patricia Heyn, Janet Kelso
Plos One|December 1, 2020
The impact of different negative training data on regulatory sequence predictionsLouisa-Marie Krützfeldt, Max Schubach, Martin Kircher
Genome Medicine|February 23, 2021
CADD-Splice-improving genome-wide variant effect prediction using deep learning-derived splice scoresPhilipp Rentzsch, Max Schubach, Jay Shendure, et al.
Bioinformatics (Oxford, England)|March 9, 2013
freeIbis: an efficient basecaller with calibrated quality scores for Illumina sequencersGabriel Renaud, Martin Kircher, Udo Stenzel, et al.
Gigascience|December 20, 2024
cfDNA UniFlow: a unified preprocessing pipeline for cell-free DNA data from liquid biopsiesSebastian Röner, Lea Burkard, Michael R Speicher, et al.
BMC Biology|November 20, 2019
Concurrent genome and epigenome editing by CRISPR-mediated sequence replacementJes Alexander, Gregory M Findlay, Martin Kircher, et al.
Pageof 9

Showing results (11-20 of 89) with videos related to

Sort By:
Pageof 9
Gigascience|April 21, 2023
The Regulatory Mendelian Mutation score for GRCh38Max Schubach, Lusiné Nazaretyan, Martin Kircher
Nucleic Acids Research|October 25, 2011
Double indexing overcomes inaccuracies in multiplex sequencing on the Illumina platformMartin Kircher, Susanna Sawyer, Matthias Meyer
Plos Computational Biology|June 5, 2020
HemoMIPs-Automated analysis and result reporting pipeline for targeted sequencing dataPhilip Kleinert, Beth Martin, Martin Kircher
Genome Medicine|August 4, 2025
varCADD: large sets of standing genetic variation enable genome-wide pathogenicity predictionLusiné Nazaretyan, Philipp Rentzsch, Martin Kircher
BMC Genomics|August 2, 2011
Addressing challenges in the production and analysis of illumina sequencing dataMartin Kircher, Patricia Heyn, Janet Kelso
Plos One|December 1, 2020
The impact of different negative training data on regulatory sequence predictionsLouisa-Marie Krützfeldt, Max Schubach, Martin Kircher
Genome Medicine|February 23, 2021
CADD-Splice-improving genome-wide variant effect prediction using deep learning-derived splice scoresPhilipp Rentzsch, Max Schubach, Jay Shendure, et al.
Bioinformatics (Oxford, England)|March 9, 2013
freeIbis: an efficient basecaller with calibrated quality scores for Illumina sequencersGabriel Renaud, Martin Kircher, Udo Stenzel, et al.
Gigascience|December 20, 2024
cfDNA UniFlow: a unified preprocessing pipeline for cell-free DNA data from liquid biopsiesSebastian Röner, Lea Burkard, Michael R Speicher, et al.
BMC Biology|November 20, 2019
Concurrent genome and epigenome editing by CRISPR-mediated sequence replacementJes Alexander, Gregory M Findlay, Martin Kircher, et al.
Pageof 9