Результати пошуку - Shane McCarthy
- Показ 1 - 20 результатів із 63
- На наступну сторінку
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1
BCFtools/csq: haplotype-aware variant consequences за авторством Petr Danecek, Shane McCarthy
Опубліковано 2017Artigo -
2
YaHS: yet another Hi-C scaffolding tool за авторством Chenxi Zhou, Shane McCarthy, Richard Durbin
Опубліковано 2022Pré-impressão -
3
YaHS: yet another Hi-C scaffolding tool за авторством Chenxi Zhou, Shane McCarthy, Richard Durbin
Опубліковано 2022Artigo -
4
Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders за авторством Jonathan Sebat, Deborah L. Levy, Shane McCarthy
Опубліковано 2009Revisão -
5
Oatk: a de novo assembly tool for complex plant organelle genomes за авторством Chenxi Zhou, Max R. Brown, Mark Blaxter, Shane McCarthy, Richard Durbin
Опубліковано 2024Pré-impressão -
6
Identifying and removing haplotypic duplication in primary genome assemblies за авторством Dengfeng Guan, Shane McCarthy, Jonathan Wood, Kerstin Howe, Yadong Wang, Richard Durbin
Опубліковано 2020Artigo -
7
A calibrated human Y-chromosomal phylogeny based on resequencing за авторством Wei Wei, Qasim Ayub, Yuan Chen, Shane McCarthy, Yiping Hou, Ignazio Carbone, Yali Xue, Chris Tyler‐Smith
Опубліковано 2012Artigo -
8
Twelve years of SAMtools and BCFtools за авторством Petr Danecek, James Bonfield, Jennifer Liddle, John Marshall, Valeriu Ohan, Martin Pollard, Andrew Whitwham, Thomas Keane, Shane McCarthy, Robert M. Davies, Heng Li
Опубліковано 2021Artigo -
9
Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom за авторством Himanshu Chheda, Priit Palta, Matti Pirinen, Shane McCarthy, Klaudia Walter, Seppo Koskinen, Veikko Salomaa, Mark J. Daly, Richard Durbin, Aarno Palotie, Tero Aittokallio, Samuli Ripatti
Опубліковано 2017Artigo -
10
MitoHiFi: a python pipeline for mitochondrial genome assembly from PacBio High Fidelity reads за авторством Marcela Uliano‐Silva, João Gabriel R. N. Ferreira, Ksenia Krasheninnikova, Giulio Formenti, Linelle Abueg, James Torrance, Eugene W. Myers, Richard Durbin, Mark Blaxter, Shane McCarthy
Опубліковано 2022Pré-impressão -
11
Modelling schizophrenia using human induced pluripotent stem cells за авторством Kristen Brennand, Anthony Simone, Jessica Jou, Chelsea Gelboin-Burkhart, Ngoc Tran, Sarah Sangar, Yan Li, Yangling Mu, Gong Chen, Diana Yu, Shane McCarthy, Jonathan Sebat, Fred H. Gage
Опубліковано 2011Artigo -
12
Reference-based phasing using the Haplotype Reference Consortium panel за авторством Po‐Ru Loh, Petr Danecek, Pier Francesco Palamara, Christian Fuchsberger, Yakir Reshef, Hilary K. Finucane, Sebastian Schoenherr, Lukas Forer, Shane McCarthy, Gonçalo R. Abecasis, Richard Durbin, Alkes L. Price
Опубліковано 2016Artigo -
13
Reference-based phasing using the Haplotype Reference Consortium panel за авторством Po‐Ru Loh, Petr Danecek, Pier Francesco Palamara, Christian Fuchsberger, Yakir Reshef, Hilary K. Finucane, Sebastian Schoenherr, Lukas Forer, Shane McCarthy, Gonçalo R. Abecasis, Richard Durbin, Alkes L. Price
Опубліковано 2016Pré-impressão -
14
A Genetic Basis of Susceptibility to Acute Pyelonephritis за авторством Ann-Charlotte Lundstedt, Shane McCarthy, Mattias C. U. Gustafsson, Gabriela Godaly, Ulf Jodal, Diana Karpman, Irene Leijonhufvud, C. Gerard van der Linden, Jeanette Martinell, Bryndís Ragnarsdóttir, Martin Samuelsson, Lennart Truedsson, Björn Andersson, Catharina Svanborg
Опубліковано 2007Artigo -
15
Deep Roots for Aboriginal Australian Y Chromosomes за авторством Anders Bergström, Nano Nagle, Yuan Chen, Shane McCarthy, Martin Pollard, Qasim Ayub, Stephen Wilcox, Leah Wilcox, Roland A.H. van Oorschot, Peter McAllister, Lesley Williams, Yali Xue, R. John Mitchell, Chris Tyler‐Smith
Опубліковано 2016Artigo -
16
Genomic evidence reveals three W-autosome fusions in Heliconius butterflies за авторством Nicol Rueda‐M, Carolina Pardo‐Díaz, Gabriela Montejo‐Kovacevich, W. Owen McMillan, Krzysztof M. Kozak, Carlos F. Arias, Jonathan Stuart Ready, Shane McCarthy, Richard Durbin, Chris D. Jiggins, Joana I. Meier, Camilo Salazar
Опубліковано 2024Artigo -
17
Reduced transcript expression of genes affected by inherited and de novo CNVs in autism за авторством Alex S. Nord, Wendy Roeb, Diane E. Dickel, Tom Walsh, Mary Kusenda, Kristen Lewis O’Connor, Dheeraj Malhotra, Shane McCarthy, Sunday M. Stray, Susan Taylor, Jonathan Sebat, Bryan H. King, Mary‐Claire King, Jon McClellan
Опубліковано 2011Artigo -
18
Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51 за авторством Tom Walsh, Sarah B. Pierce, Danielle R. Lenz, Zippora Brownstein, Orit Dagan‐Rosenfeld, Hashem Shahin, Wendy Roeb, Shane McCarthy, Alex S. Nord, Carlos R. Gordon, Ziva Ben‐Neriah, Jonathan Sebat, Moien Kanaan, Ming K. Lee, Moshe Frydman, Mary‐Claire King, Karen B. Avraham
Опубліковано 2010Artigo -
19
Characterization of molecular and cellular phenotypes associated with a heterozygous CNTNAP2 deletion using patient-derived hiPSC neural cells за авторством Inkyu S Lee, Claudia M.B. Carvalho, Panagiotis Douvaras, Seok‐Man Ho, Brigham J. Hartley, Luciana W. Zuccherato, Ian Ladran, Arthur J. Siegel, Shane McCarthy, Dheeraj Malhotra, Jonathan Sebat, Judith L. Rapoport, Valentina Fossati, James R. Lupski, Deborah L. Levy, Kristen Brennand
Опубліковано 2015Artigo -
20
Use of whole genome sequencing to estimate the contribution of immune evasion and waning immunity to decreasing COVID-19 vaccine effectiveness during alpha and delta variant waves за авторством Margaret L. Lind, Richard Copin, Shane McCarthy, Andreas Coppi, Fred Warner, David Ferguson, Chelsea Duckwall, Ryan Borg, M. Catherine Muenker, John D. Overton, Sara Hamon, Anbo Zhou, Derek A. T. Cummings, Albert I. Ko, Jennifer D. Hamilton, Wade L. Schulz, Matt T. Hitchings
Опубліковано 2022Pré-impressão
Інструменти для пошуку:
Пов'язані теми
Biology
Genetics
Gene
Genome
Medicine
Computational biology
Genotype
Single-nucleotide polymorphism
Internal medicine
Computer science
Evolutionary biology
1000 Genomes Project
Population
Disease
Gene expression
Allele
Copy-number variation
Demography
Haplotype
Mutation
Phenotype
Sociology
Genetic association
Genome-wide association study
Imputation (statistics)
Machine learning
Missing data
Psychiatry
Allele frequency
Transcriptome