Posted
1st
February
2022
Posted
28th
January
2022
Global barriers to genomics - Malaysian Epilepsy Conference
Posted
18th
January
2022
Added fear of mortality for rare caregivers
Posted
6th
January
2022
Enabling Genomic Medicine in China
Posted
5th
January
2022
Bringing genomics into the heart of healthcare
Posted
17th
December
2021
Full Speed Ahead for FAM177A1: Two Siblings' Diagnostic Odyssey
Posted
15th
December
2021
Webinar highlights of 2021
Posted
9th
December
2021
Rare disease and diagnosis in 2021
Posted
7th
December
2021
Best practices in automatable clinical decision support workflows
Posted
25th
November
2021
Whole Genome Sequencing at Birth: What Should Be Looked For?
Posted
24th
November
2021
Why choose a professional solution for your genomic data analysis?
Posted January
Jan
28th
2022
Global barriers to genomics - Malaysian Epilepsy Conference
Posted January
Jan
18th
2022
Added fear of mortality for rare caregivers
Posted January
Jan
6th
2022
Enabling Genomic Medicine in China
Posted January
Jan
5th
2022
Bringing genomics into the heart of healthcare
Posted December
Dec
17th
2021
Full Speed Ahead for FAM177A1: Two Siblings' Diagnostic Odyssey
Posted December
Dec
15th
2021
Webinar highlights of 2021
Posted December
Dec
9th
2021
Rare disease and diagnosis in 2021
Posted December
Dec
7th
2021
Best practices in automatable clinical decision support workflows
Posted November
Nov
25th
2021
Whole Genome Sequencing at Birth: What Should Be Looked For?
Posted November
Nov
24th
2021
