[HTML][HTML] Prognostic genetic markers for thrombosis in COVID-19 patients: a focused analysis on D-dimer, homocysteine and thromboembolism
COVID-19 is caused by Severe Acute Respiratory Syndrome Coronavirus-2, which has
infected over thirty eight million individuals worldwide. Emerging evidence indicates that …
infected over thirty eight million individuals worldwide. Emerging evidence indicates that …
[HTML][HTML] A review of ancestrality and admixture in Latin America and the caribbean focusing on native American and African descendant populations
Genomics can reveal essential features about the demographic evolution of a population
that may not be apparent from historical elements. In recent years, there has been a …
that may not be apparent from historical elements. In recent years, there has been a …
Fast and accurate genomic analyses using genome graphs
The human reference genome serves as the foundation for genomics by providing a scaffold
for alignment of sequencing reads, but currently only reflects a single consensus haplotype …
for alignment of sequencing reads, but currently only reflects a single consensus haplotype …
[HTML][HTML] SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
A Ameur, J Dahlberg, P Olason, F Vezzi… - European Journal of …, 2017 - nature.com
Here we describe the SweGen data set, a comprehensive map of genetic variation in the
Swedish population. These data represent a basic resource for clinical genetics laboratories …
Swedish population. These data represent a basic resource for clinical genetics laboratories …
IndiGenomes: a comprehensive resource of genetic variants from over 1000 Indian genomes
With the advent of next-generation sequencing, large-scale initiatives for mining whole
genomes and exomes have been employed to better understand global or population-level …
genomes and exomes have been employed to better understand global or population-level …
[HTML][HTML] Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants
Whole-genome sequencing (WGS) is a fundamental technology for research to advance
precision medicine, but the limited availability of portable and user-friendly workflows for …
precision medicine, but the limited availability of portable and user-friendly workflows for …
[HTML][HTML] Point-of-care whole-exome sequencing of idiopathic male infertility
KA Fakhro, H Elbardisi, M Arafa, A Robay… - Genetics in …, 2018 - Elsevier
Purpose Nonobstructive azoospermia (NOA) affects 1% of the male population; however,
despite state-of-the-art clinical assessment, for most patients the cause is unknown. We …
despite state-of-the-art clinical assessment, for most patients the cause is unknown. We …
Qatar genome: Insights on genomics from the Middle East
H Mbarek, G Devadoss Gandhi, S Selvaraj… - Human …, 2022 - Wiley Online Library
Despite recent biomedical breakthroughs and large genomic studies growing momentum,
the Middle Eastern population, home to over 400 million people, is underrepresented in the …
the Middle Eastern population, home to over 400 million people, is underrepresented in the …
Origin matters: Using a local reference genome improves measures in population genomics
DMJ Thorburn, K Sagonas… - Molecular ecology …, 2023 - Wiley Online Library
Genome sequencing enables answering fundamental questions about the genetic basis of
adaptation, population structure and epigenetic mechanisms. Yet, we usually need a …
adaptation, population structure and epigenetic mechanisms. Yet, we usually need a …
[HTML][HTML] Thousands of Qatari genomes inform human migration history and improve imputation of Arab haplotypes
RM Razali, J Rodriguez-Flores, M Ghorbani… - Nature …, 2021 - nature.com
Arab populations are largely understudied, notably their genetic structure and history. Here
we present an in-depth analysis of 6,218 whole genomes from Qatar, revealing extensive …
we present an in-depth analysis of 6,218 whole genomes from Qatar, revealing extensive …