Search

Author/Creator Becq, Jennifer

1. Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100, 000 Genomes Project. (October 2018)

Authors:
Robbe, Pauline; Popitsch, Niko; Knight, Samantha; Antoniou, Pavlos; Becq, Jennifer; He, Miao; Kanapin, Alexander; Samsonova, Anastasia; Vavoulis, Dimitrios; Ross, Mark; Kingsbury, Zoya; Cabes, Maite; Ramos, Sara; Page, Suzanne; Dreau, Helene; Ridout, Kate; Jones, Louise; Tuff-Lacey, Alice; Hender...
Journal:
Genetics in medicine
Issue:
Volume 20:Number 10(2018)
Page Start:
1196
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Clinical‐grade validation of whole genome sequencing reveals robust detection of low‐frequency variants and copy number alterations in CLL. (29th May 2018)

Authors:
Klintman, Jenny; Barmpouti, Katerina; Knight, Samantha J. L.; Robbe, Pauline; Dreau, Hélène; Clifford, Ruth; Ridout, Kate; Burns, Adam; Timbs, Adele; Bruce, David; Antoniou, Pavlos; Sosinsky, Alona; Becq, Jennifer; Bentley, David; Hillmen, Peter; Taylor, Jenny C.; Caulfield, Mark; Schuh, Anna H.
Journal:
British journal of haematology
Issue:
Volume 182:Number 3(2018)
Page Start:
412
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

Limit your search