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1.
A comprehensive benchmarking of WGS-based deletion structural variant callers.
Brief Bioinform
; 23(4)2022 07 18.
Article
in English
| MEDLINE | ID: mdl-35753701
2.
CONGA: Copy number variation genotyping in ancient genomes and low-coverage sequencing data.
PLoS Comput Biol
; 18(12): e1010788, 2022 12.
Article
in English
| MEDLINE | ID: mdl-36516232
3.
Discovery of tandem and interspersed segmental duplications using high-throughput sequencing.
Bioinformatics
; 35(20): 3923-3930, 2019 10 15.
Article
in English
| MEDLINE | ID: mdl-30937433
4.
Toolkit for automated and rapid discovery of structural variants.
Methods
; 129: 3-7, 2017 10 01.
Article
in English
| MEDLINE | ID: mdl-28583483
5.
Long-read sequencing and structural variant characterization in 1,019 samples from the 1000 Genomes Project.
bioRxiv
; 2024 Apr 20.
Article
in English
| MEDLINE | ID: mdl-38659906
6.
Metabolic independence drives gut microbial colonization and resilience in health and disease.
Genome Biol
; 24(1): 78, 2023 04 17.
Article
in English
| MEDLINE | ID: mdl-37069665
7.
MTaxi: A comparative tool for taxon identification of ultra low coverage ancient genomes.
Open Res Eur
; 2: 100, 2022.
Article
in English
| MEDLINE | ID: mdl-37829208
8.
An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates.
F1000Res
; 10: 246, 2021.
Article
in English
| MEDLINE | ID: mdl-34621504
9.
Author Correction: A robust benchmark for detection of germline large deletions and insertions.
Nat Biotechnol
; 38(11): 1357, 2020 Nov.
Article
in English
| MEDLINE | ID: mdl-32699374
10.
A robust benchmark for detection of germline large deletions and insertions.
Nat Biotechnol
; 38(11): 1347-1355, 2020 11.
Article
in English
| MEDLINE | ID: mdl-32541955
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