AW: Short-read data can lead to false positives/false negatives, Genetics in Medicine paper: https://t.co/DcJcb2blei #PBUGM
RT @GIMJournal: A resource for clinical next-generation sequencing. See Mandelker et al https://t.co/aPs7rUwUSR https://t.co/uQIfXo2ZAN
RT @GIMJournal: A resource for clinical next-generation sequencing. See Mandelker et al https://t.co/aPs7rUwUSR https://t.co/uQIfXo2ZAN
RT @GIMJournal: A resource for clinical next-generation sequencing. See Mandelker et al https://t.co/aPs7rUwUSR https://t.co/uQIfXo2ZAN
Useful resource for exome sequencing from @BirgitFunke and team: https://t.co/5LNt0rBb5q
RT @GIMJournal: A resource for clinical next-generation sequencing. See Mandelker et al https://t.co/aPs7rUwUSR https://t.co/uQIfXo2ZAN
A resource for clinical next-generation sequencing. See Mandelker et al https://t.co/aPs7rUwUSR https://t.co/uQIfXo2ZAN
RT @euanashley: Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical NGS https://t.co/tKU1XNzqi5
Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical NGS https://t.co/tKU1XNzqi5
Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical NGS https://t.co/heqOy1qTLE
Navigating highly homologous genes in diagnostic setting: a resource for clinical next-generation sequencing https://t.co/v3jvJ3dJ7x
Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical NGS https://t.co/rik6Qj083q
Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical next-generation… https://t.co/lb7Fulxifq
great, even the url of the resource is behind a paywall: Navigating highly homologous genes in a molecular diagn... https://t.co/sE6kGSllfz