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Michelle D Noyes

Showing results (1-10 of 11) with videos related to

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Biorxiv : the Preprint Server for Biology|January 8, 2024
Effects of parental age and polymer composition on short tandem repeat <i>de novo</i> mutation ratesMichael E Goldberg, Michelle D Noyes, Evan E Eichler, et al.
Genetics|February 1, 2024
Effects of parental age and polymer composition on short tandem repeat de novo mutation ratesMichael E Goldberg, Michelle D Noyes, Evan E Eichler, et al.
Biorxiv : the Preprint Server for Biology|August 12, 2025
Long-read sequencing of trios reveals increased germline and postzygotic mutation rates in repetitive DNAMichelle D Noyes, Yang Sui, Youngjun Kwon, et al.
Nature Communications|March 10, 2026
Long-read sequencing of families reveals increased germline and postzygotic mutation rates in repetitive DNAMichelle D Noyes, Yang Sui, Youngjun Kwon, et al.
Biorxiv : the Preprint Server for Biology|December 25, 2025
Human acrocentric chromosome short arm <i>de novo</i> mutation and recombinationJiadong Lin, F Kumara Mastrorosa, Michelle D Noyes, et al.
American Journal of Human Genetics|March 15, 2022
Familial long-read sequencing increases yield of de novo mutationsMichelle D Noyes, William T Harvey, David Porubsky, et al.
Nature Communications|January 23, 2026
Using the linear references from the pangenome to discover missing autism variantsYang Sui, Jiadong Lin, Michelle D Noyes, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Pangenome discovery of missing autism variantsYang Sui, Jiadong Lin, Michelle D Noyes, et al.
Biorxiv : the Preprint Server for Biology|August 16, 2024
A familial, telomere-to-telomere reference for human <i>de novo</i> mutation and recombination from a four-generation pedigreeDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.
Biorxiv : the Preprint Server for Biology|February 27, 2026
Donor-specific assemblies enhance somatic structural variant detection in complex genomic regionsTaralynn M Mack, Jiadong Lin, Luyao Ren, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Biorxiv : the Preprint Server for Biology|January 8, 2024
Effects of parental age and polymer composition on short tandem repeat <i>de novo</i> mutation ratesMichael E Goldberg, Michelle D Noyes, Evan E Eichler, et al.
Genetics|February 1, 2024
Effects of parental age and polymer composition on short tandem repeat de novo mutation ratesMichael E Goldberg, Michelle D Noyes, Evan E Eichler, et al.
Biorxiv : the Preprint Server for Biology|August 12, 2025
Long-read sequencing of trios reveals increased germline and postzygotic mutation rates in repetitive DNAMichelle D Noyes, Yang Sui, Youngjun Kwon, et al.
Nature Communications|March 10, 2026
Long-read sequencing of families reveals increased germline and postzygotic mutation rates in repetitive DNAMichelle D Noyes, Yang Sui, Youngjun Kwon, et al.
Biorxiv : the Preprint Server for Biology|December 25, 2025
Human acrocentric chromosome short arm <i>de novo</i> mutation and recombinationJiadong Lin, F Kumara Mastrorosa, Michelle D Noyes, et al.
American Journal of Human Genetics|March 15, 2022
Familial long-read sequencing increases yield of de novo mutationsMichelle D Noyes, William T Harvey, David Porubsky, et al.
Nature Communications|January 23, 2026
Using the linear references from the pangenome to discover missing autism variantsYang Sui, Jiadong Lin, Michelle D Noyes, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Pangenome discovery of missing autism variantsYang Sui, Jiadong Lin, Michelle D Noyes, et al.
Biorxiv : the Preprint Server for Biology|August 16, 2024
A familial, telomere-to-telomere reference for human <i>de novo</i> mutation and recombination from a four-generation pedigreeDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.
Biorxiv : the Preprint Server for Biology|February 27, 2026
Donor-specific assemblies enhance somatic structural variant detection in complex genomic regionsTaralynn M Mack, Jiadong Lin, Luyao Ren, et al.
Pageof 2