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Plos Computational Biology|June 5, 2020
HemoMIPs-Automated analysis and result reporting pipeline for targeted sequencing dataPhilip Kleinert, Beth Martin, Martin KircherGenome Research|February 24, 2022
A framework to score the effects of structural variants in health and diseasePhilip Kleinert, Martin KircherNature Methods|October 13, 2020
A systematic evaluation of the design and context dependencies of massively parallel reporter assaysJason C Klein, Vikram Agarwal, Fumitaka Inoue, et al.Methods in Molecular Biology (Clifton, N.J.)|January 13, 2012
Analysis of high-throughput ancient DNA sequencing dataMartin KircherGenome Research|November 11, 2016
A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activityFumitaka Inoue, Martin Kircher, Beth Martin, et al.Cold Spring Harbor Protocols|June 3, 2010
Illumina sequencing library preparation for highly multiplexed target capture and sequencingMatthias Meyer, Martin KircherNature Genetics|July 30, 2015
Running spell-check to identify regulatory variantsMartin Kircher, Jay ShendureBioessays : News and Reviews in Molecular, Cellular and Developmental Biology|May 21, 2010
High-throughput DNA sequencing--concepts and limitationsMartin Kircher, Janet KelsoNature Communications|August 10, 2019
Saturation mutagenesis of twenty disease-associated regulatory elements at single base-pair resolutionMartin Kircher, Chenling Xiong, Beth Martin, et al.Cold Spring Harbor Molecular Case Studies|April 28, 2022
Computational and experimental methods for classifying variants of unknown clinical significanceMalte Spielmann, Martin KircherPageof 16