Pesquisa | Portal de Pesquisa da BVS Enfermagem

1.

Mapping of sister chromatid exchange events and genome alterations in single cells.

Hamadeh, Zeid; Hanlon, Vincent; Lansdorp, Peter M.

Methods ; 204: 64-72, 2022 08.

Artigo em Inglês | MEDLINE | ID: mdl-35483548

2.

A survey of current methods to detect and genotype inversions.

Hanlon, Vincent C T; Lansdorp, Peter M; Guryev, Victor.

Hum Mutat ; 43(11): 1576-1589, 2022 11.

Artigo em Inglês | MEDLINE | ID: mdl-36047337

3.

InvertypeR: Bayesian inversion genotyping with Strand-seq data.

Hanlon, Vincent C T; Mattsson, Carl-Adam; Spierings, Diana C J; Guryev, Victor; Lansdorp, Peter M.

BMC Genomics ; 22(1): 582, 2021 Jul 31.

Artigo em Inglês | MEDLINE | ID: mdl-34332539

4.

Ten million and counting.

Hanlon, Vincent.

CMAJ ; 195(37): E1277-E1278, 2023 09 25.

Artigo em Inglês | MEDLINE | ID: mdl-37748780

5.

Dix millions de fois et plus encore!

Hanlon, Vincent.

CMAJ ; 195(43): E1496-E1498, 2023 11 06.

Artigo em Francês | MEDLINE | ID: mdl-37931946

6.

Chromosome-Length Haplotypes with StrandPhaseR and Strand-seq.

Hanlon, Vincent C T; Porubsky, David; Lansdorp, Peter M.

Methods Mol Biol ; 2590: 183-200, 2023.

Artigo em Inglês | MEDLINE | ID: mdl-36335500

7.

Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq.

Akbari, Vahid; Hanlon, Vincent C T; O'Neill, Kieran; Lefebvre, Louis; Schrader, Kasmintan A; Lansdorp, Peter M; Jones, Steven J M.

Cell Genom ; 3(1): 100233, 2023 Jan 11.

Artigo em Inglês | MEDLINE | ID: mdl-36777186

8.

Construction of Strand-seq libraries in open nanoliter arrays.

Hanlon, Vincent C T; Chan, Daniel D; Hamadeh, Zeid; Wang, Yanni; Mattsson, Carl-Adam; Spierings, Diana C J; Coope, Robin J N; Lansdorp, Peter M.

Cell Rep Methods ; 2(1): 100150, 2022 01 24.

Artigo em Inglês | MEDLINE | ID: mdl-35474869

9.

Benchmarking challenging small variants with linked and long reads.

Wagner, Justin; Olson, Nathan D; Harris, Lindsay; Khan, Ziad; Farek, Jesse; Mahmoud, Medhat; Stankovic, Ana; Kovacevic, Vladimir; Yoo, Byunggil; Miller, Neil; Rosenfeld, Jeffrey A; Ni, Bohan; Zarate, Samantha; Kirsche, Melanie; Aganezov, Sergey; Schatz, Michael C; Narzisi, Giuseppe; Byrska-Bishop, Marta; Clarke, Wayne; Evani, Uday S; Markello, Charles; Shafin, Kishwar; Zhou, Xin; Sidow, Arend; Bansal, Vikas; Ebert, Peter; Marschall, Tobias; Lansdorp, Peter; Hanlon, Vincent; Mattsson, Carl-Adam; Barrio, Alvaro Martinez; Fiddes, Ian T; Xiao, Chunlin; Fungtammasan, Arkarachai; Chin, Chen-Shan; Wenger, Aaron M; Rowell, William J; Sedlazeck, Fritz J; Carroll, Andrew; Salit, Marc; Zook, Justin M.

Cell Genom ; 2(5)2022 May.

Artigo em Inglês | MEDLINE | ID: mdl-36452119

10.

Somatic mutations substantially increase the per-generation mutation rate in the conifer Picea sitchensis.

Hanlon, Vincent C T; Otto, Sarah P; Aitken, Sally N.

Evol Lett ; 3(4): 348-358, 2019 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-31388445

11.

Blue gown, white coat.

Hanlon, Vincent.

CJEM ; 5(3): 213-4, 2003 May.

Artigo em Inglês | MEDLINE | ID: mdl-17472785

12.

Music in my ERs.

Hanlon, Vincent.

CJEM ; 4(5): 369-70, 2002 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-17608984

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Mapping of sister chromatid exchange events and genome alterations in single cells.

A survey of current methods to detect and genotype inversions.

InvertypeR: Bayesian inversion genotyping with Strand-seq data.

Ten million and counting.

Dix millions de fois et plus encore!

Chromosome-Length Haplotypes with StrandPhaseR and Strand-seq.

Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq.

Construction of Strand-seq libraries in open nanoliter arrays.

Benchmarking challenging small variants with linked and long reads.

Somatic mutations substantially increase the per-generation mutation rate in the conifer Picea sitchensis.

Blue gown, white coat.

Music in my ERs.