Family-based Genetic Analysis

Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD (2024)
Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing
Eur J Hum Genet (in press)
DOI 10.1038/s41431-023-01519-1, PubMed 38172175

Carrizosa C, Undlien DE, Vigeland MD (2024)
shinyseg: a web application for flexible cosegregation and sensitivity analysis
Bioinformatics (in press)
DOI 10.1093/bioinformatics/btae201, PubMed 38598476

Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD (2023)
A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing
Eur J Hum Genet (in press)
DOI 10.1038/s41431-023-01494-7, PubMed 38030917