Martin O Pollard
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Explore the profile of Martin O Pollard including associated specialties, affiliations and a list of published articles.
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8
Citations
4866
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Recent Articles
1.
Danecek P, Bonfield J, Liddle J, Marshall J, Ohan V, Pollard M, et al.
Gigascience
. 2021 Feb;
10(2).
PMID: 33590861
Background: SAMtools and BCFtools are widely used programs for processing and analysing high-throughput sequencing data. They include tools for file format conversion and manipulation, sorting, querying, statistics, variant calling, and...
2.
Sallah N, Miley W, Labo N, Carstensen T, Fatumo S, Gurdasani D, et al.
Nat Commun
. 2020 Aug;
11(1):3849.
PMID: 32737300
Kaposi's sarcoma-associated herpesvirus (KSHV) and Epstein-Barr Virus (EBV) establish life-long infections and are associated with malignancies. Striking geographic variation in incidence and the fact that virus alone is insufficient to...
3.
Gurdasani D, Carstensen T, Fatumo S, Chen G, Franklin C, Prado-Martinez J, et al.
Cell
. 2019 Nov;
179(4):984-1002.e36.
PMID: 31675503
Genomic studies in African populations provide unique opportunities to understand disease etiology, human diversity, and population history. In the largest study of its kind, comprising genome-wide data from 6,400 individuals...
4.
Gilly A, Southam L, Suveges D, Kuchenbaecker K, Moore R, Melloni G, et al.
Bioinformatics
. 2018 Dec;
35(15):2555-2561.
PMID: 30576415
Motivation: Very low-depth sequencing has been proposed as a cost-effective approach to capture low-frequency and rare variation in complex trait association studies. However, a full characterization of the genotype quality...
5.
Pollard M, Gurdasani D, Mentzer A, Porter T, Sandhu M
Hum Mol Genet
. 2018 May;
27(R2):R234-R241.
PMID: 29767702
In recent years long-read technologies have moved from being a niche and specialist field to a point of relative maturity likely to feature frequently in the genomic landscape. Analogous to...
6.
Sifrim A, Hitz M, Wilsdon A, Breckpot J, Al Turki S, Thienpont B, et al.
Nat Genet
. 2016 Aug;
48(9):1060-5.
PMID: 27479907
Congenital heart defects (CHDs) have a neonatal incidence of 0.8-1% (refs. 1,2). Despite abundant examples of monogenic CHD in humans and mice, CHD has a low absolute sibling recurrence risk...
7.
Bergstrom A, Nagle N, Chen Y, McCarthy S, Pollard M, Ayub Q, et al.
Curr Biol
. 2016 Mar;
26(6):809-13.
PMID: 26923783
Australia was one of the earliest regions outside Africa to be colonized by fully modern humans, with archaeological evidence for human presence by 47,000 years ago (47 kya) widely accepted...
8.
Gurdasani D, Carstensen T, Tekola-Ayele F, Pagani L, Tachmazidou I, Hatzikotoulas K, et al.
Nature
. 2014 Dec;
517(7534):327-32.
PMID: 25470054
Given the importance of Africa to studies of human origins and disease susceptibility, detailed characterization of African genetic diversity is needed. The African Genome Variation Project provides a resource with...