Posted
25th
November
2022
Posted
28th
January
2022
Global barriers to genomics - Malaysian Epilepsy Conference
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
11th
November
2021
Opening the Black Box: Telling the Story of a Genomic Diagnosis
Posted
11th
November
2021
100k Genomes Pilot on Rare Disease Diagnosis in Healthcare
Posted
15th
October
2021
Enabling Genomic Medicine 2021
Posted
25th
August
2021
Automating Clinical Genomic Analysis & Reporting for Rapid NGS Results
Posted
6th
August
2021
Science, genomics hope and a father's love
Posted
25th
November
2022
The Real Costs of Rare Disease
Posted January
Jan
28th
2022
Global barriers to genomics - Malaysian Epilepsy Conference
Posted November
Nov
25th
2021
Whole Genome Sequencing at Birth: What Should Be Looked For?
Posted November
Nov
24th
2021
Why choose a professional solution for your genomic data analysis?
Posted November
Nov
11th
2021
Opening the Black Box: Telling the Story of a Genomic Diagnosis
Posted November
Nov
11th
2021
100k Genomes Pilot on Rare Disease Diagnosis in Healthcare
Posted October
Oct
15th
2021
Enabling Genomic Medicine 2021
Posted August
Aug
25th
2021
Automating Clinical Genomic Analysis & Reporting for Rapid NGS Results
Posted August
Aug
6th
2021