Genomics in action

0-9

• 100,000 Genomes Project Genomics in action

A

B

C

• CanRisk Genomics in action
• Clinical genetics services map Genomics in action
• Clinical trials in cancer Genomics in action
• The consent conversation for genomic testing Genomics in action

D

E

F

G

• Genomic Laboratory Hubs Genomics in action
• Genomic testing in the devolved nations Genomics in action
• The Generation Study Genomics in action
• The genomics multidisciplinary team meeting (MDT) in rare disease Genomics in action

H

• How to complete a record of discussion form Genomics in action
• How to complete a test order form for whole genome sequencing Genomics in action
• How to request a skeletal survey Genomics in action
• The Human Genome Project Genomics in action

I

• Incidental findings Genomics in action

J

K

L

M

• Mainstreaming cancer susceptibility gene testing Genomics in action
• Mental health and rare disease Genomics in action

N

• NHS Genomic Medicine Service Signed Off Panels Resource Genomics in action
• The genomic testing pathway in rare disease Genomics in action
• The National Genomic Test Directory Genomics in action

O

P

• Point-of-care pharmacogenomic testing Genomics in action
• Rare disease patient advocacy groups Genomics in action

Q

R

• R14: Acutely unwell children with a likely monogenic disorder (rapid genome testing) Genomics in action
• Roles in clinical genetics Genomics in action

S

• Samples for genomic testing in rare disease Genomics in action

T

U

V

• Variant of uncertain significance (VUS) Genomics in action

W

X

Y

Z