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Tom Mokveld

Showing results (1-10 of 16) with videos related to

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Diagnostics (Basel, Switzerland)|January 21, 2022
WisecondorFF: Improved Fetal Aneuploidy Detection from Shallow WGS through Fragment Length AnalysisTom Mokveld, Zaid Al-Ars, Erik A Sistermans, et al.
Plos One|April 14, 2023
A comprehensive performance analysis of sequence-based within-sample testing NIPT methodsTom Mokveld, Zaid Al-Ars, Erik A Sistermans, et al.
Genome Biology|March 13, 2020
CHOP: haplotype-aware path indexing in population graphsTom Mokveld, Jasper Linthorst, Zaid Al-Ars, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|February 22, 2024
Evaluating the effectiveness of pre-operative diagnosis of ovarian cancer using minimally invasive liquid biopsies by combining serum human epididymis protein 4 and cell-free DNA in patients with an ovarian massDuco H K Gaillard, Pien Lof, Erik A Sistermans, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2026
A computational model for quantifying instability of tandem repeats across the genomeEgor Dolzhenko, Adam English, Tom Mokveld, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
A family portrait of the genomic factors shaping tandem repeat mutagenesisThomas A Sasani, Michael E Goldberg, Akshay K Avvaru, et al.
American Journal of Human Genetics|January 14, 2025
HiFi long-read genomes for difficult-to-detect, clinically relevant variantsWolfram Höps, Marjan M Weiss, Ronny Derks, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2023
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in <i>AFF3</i> as a significant cause of intellectual disabilityBharati Jadhav, Paras Garg, Joke J F A van Vugt, et al.
Nature Genetics|September 23, 2024
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disabilityBharati Jadhav, Paras Garg, Joke J F A van Vugt, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|April 14, 2025
Evaluating the effectiveness of pre-operative diagnosis of ovarian cancer using minimally invasive liquid biopsies by combining serum human epididymis protein 4 and cell-free DNA in patients with an ovarian massDuco H K Gaillard, Pien Lof, Erik A Sistermans, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Diagnostics (Basel, Switzerland)|January 21, 2022
WisecondorFF: Improved Fetal Aneuploidy Detection from Shallow WGS through Fragment Length AnalysisTom Mokveld, Zaid Al-Ars, Erik A Sistermans, et al.
Plos One|April 14, 2023
A comprehensive performance analysis of sequence-based within-sample testing NIPT methodsTom Mokveld, Zaid Al-Ars, Erik A Sistermans, et al.
Genome Biology|March 13, 2020
CHOP: haplotype-aware path indexing in population graphsTom Mokveld, Jasper Linthorst, Zaid Al-Ars, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|February 22, 2024
Evaluating the effectiveness of pre-operative diagnosis of ovarian cancer using minimally invasive liquid biopsies by combining serum human epididymis protein 4 and cell-free DNA in patients with an ovarian massDuco H K Gaillard, Pien Lof, Erik A Sistermans, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2026
A computational model for quantifying instability of tandem repeats across the genomeEgor Dolzhenko, Adam English, Tom Mokveld, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
A family portrait of the genomic factors shaping tandem repeat mutagenesisThomas A Sasani, Michael E Goldberg, Akshay K Avvaru, et al.
American Journal of Human Genetics|January 14, 2025
HiFi long-read genomes for difficult-to-detect, clinically relevant variantsWolfram Höps, Marjan M Weiss, Ronny Derks, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2023
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in <i>AFF3</i> as a significant cause of intellectual disabilityBharati Jadhav, Paras Garg, Joke J F A van Vugt, et al.
Nature Genetics|September 23, 2024
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disabilityBharati Jadhav, Paras Garg, Joke J F A van Vugt, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|April 14, 2025
Evaluating the effectiveness of pre-operative diagnosis of ovarian cancer using minimally invasive liquid biopsies by combining serum human epididymis protein 4 and cell-free DNA in patients with an ovarian massDuco H K Gaillard, Pien Lof, Erik A Sistermans, et al.
Pageof 2