Correction to: Genome-wide sequencing as a first-tier screening test for short tandem repeat expansions
Genome Med
.
2021 Sep 13;13(1):151.
doi: 10.1186/s13073-021-00961-4.
Authors
Indhu-Shree Rajan-Babu
1
2
,
Junran J Peng
3
,
Readman Chiu
4
;
IMAGINE Study
;
CAUSES Study
;
Chenkai Li
4
5
,
Arezoo Mohajeri
3
,
Egor Dolzhenko
6
,
Michael A Eberle
6
,
Inanc Birol
3
4
,
Jan M Friedman
3
Collaborators
Patricia Birch
,
Madeline Couse
,
Colleen Guimond
,
Anna Lehman
,
Jill Mwenifumbo
,
Clara van Karnebeek
,
Jan Friedman
,
Shelin Adam
,
Christele Du Souich
,
Alison Elliott
,
Anna Lehman
,
Jill Mwenifumbo
,
Tanya Nelson
,
Clara van Karnebeek
,
Rajan-Babu
,
Jan Friedman
Affiliations
1
Department of Medical Genetics, University of British Columbia and Children's & Women's Hospital, Vancouver, BC, V6H3N1, Canada.
[email protected]
.
2
Department of Medical and Molecular Genetics, King's College London, Strand, London, WC2R 2LS, UK.
[email protected]
.
3
Department of Medical Genetics, University of British Columbia and Children's & Women's Hospital, Vancouver, BC, V6H3N1, Canada.
4
Canada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, BC, V5Z4S6, Canada.
5
Bioinformatics Graduate Program, University of British Columbia, Vancouver, BC, V6T1Z4, Canada.
6
Illumina Inc., San Diego, CA, 92121, USA.
PMID:
34517885
PMCID:
PMC8439056
DOI:
10.1186/s13073-021-00961-4
No abstract available
Publication types
Published Erratum