Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Audald Lloret-Villas"'
Autor:
Xena Marie Mapel, Naveen Kumar Kadri, Alexander S. Leonard, Qiongyu He, Audald Lloret-Villas, Meenu Bhati, Maya Hiltpold, Hubert Pausch
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-15 (2024)
Abstract Breeding bulls are well suited to investigate inherited variation in male fertility because they are genotyped and their reproductive success is monitored through semen analyses and thousands of artificial inseminations. However, functional
Externí odkaz:
https://doaj.org/article/4e9432c4ac32434888c08e1bec982656
Publikováno v:
Genetics Selection Evolution, Vol 55, Iss 1, Pp 1-11 (2023)
Abstract Background Low-pass sequencing followed by sequence variant genotype imputation is an alternative to the routine microarray-based genotyping in cattle. However, the impact of haplotype reference panels and their interplay with the coverage o
Externí odkaz:
https://doaj.org/article/e2318d96c8b4470992cdf72cbe38d556
Autor:
Xena Marie Mapel, Naveen Kumar Kadri, Alexander S. Leonard, Qiongyu He, Audald Lloret-Villas, Meenu Bhati, Maya Hiltpold, Hubert Pausch
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/32391ae90a1347d395b47b47e92d0815
Publikováno v:
BMC Genomics, Vol 22, Iss 1, Pp 1-17 (2021)
Abstract Background Reference-guided read alignment and variant genotyping are prone to reference allele bias, particularly for samples that are greatly divergent from the reference genome. A Hereford-based assembly is the widely accepted bovine refe
Externí odkaz:
https://doaj.org/article/98a85278c8034f1a94e944e69b11f5cc
Additional file 8 Figure S3: Density of variants deviating from Hardy-Weinberg proportion for chromosome 12. The number of variants differing from Hardy-Weinberg proportion are plotted as non-overlapping windows of 10 Kb along the autosomal sequence.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::422a93623f5d7088b0d992cec95761bc
Additional file 5 Figure S2: Density of variants across chromosomes 13 and 23. The number of variants is shown within non-overlapping windows of 10 Kb for chromosome 13 (A) and 23 (B). The x-axis indicates the length of the chromosome (in Mb). The nu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::566105a3de58d2ba287711632472a2e1
Additional file 12 Figure S4: Selective sweeps on chromosome 13. Chromosome 13 region in ARS-UCD1.2 from 10,501,688 - 12,506,844 Mb and corresponding region on UOA_Angus_1 between 71,231,671 - 73,018,009 Mb with highlighted six selective sweep region
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a3d51d13733291e9d9d4861116b053a
Publikováno v:
CBMS
The European Genome-phenome Archive (EGA) is a repository that facilitates access and management for long-term archival of human biomolecular data. The EGA is co-managed by the European Bioinformatics Institute (EBI) and the Centre for Genomic Regula
Publikováno v:
Big Data Analytics. 1
The International Symposium “Advances in Systems Biology in Neurosciences” was held in February 2015 in Geneva. A hundred scientists with a variety of expertise gathered around the theme of human brain complexity and cognitive disorders. Through
Autor:
Audald Lloret-Villas, Nick Juty, Thawfeek M. Varusai, Camille Laibe, Vijayalakshmi Chelliah, N Le Novère, Henning Hermjakob
Publikováno v:
CPT: Pharmacometrics & Systems Pharmacology
Neurodegenerative diseases are a heterogeneous group of disorders that are characterized by the progressive dysfunction and loss of neurons. Here, we distil and discuss the current state of modeling in the area of neurodegeneration, and objectively c