Using Whole Genome Sequencing (WGS) For The Undiagnosed Pediatric Patients With Rare Disease

Events

Using Whole Genome Sequencing (WGS) For The Undiagnosed Pediatric Patients With Rare Disease

  • July 20, 2023
  • Events

A/Prof Giorgia Pastorin will be hosting a seminar on 02 August 2023, 11:00am at S4, Level 5 Seminar Room and/or Zoom Session (Hybrid). The invited speaker is Dr. Kai Lee Yap and she will be sharing on Using Whole Genome Sequencing (WGS) For The Undiagnosed Pediatric Patients With Rare Disease.

Please click here to attend Zoom session

Date: 02 August 2023
Time: 11:00 am
Venue: S4, Level 5 Seminar Room / Zoom (Hybrid)

Recent Events

  • A VP4 synonymous mutation reduces enterovirus 71 replication and modulates tissue tropism

    10 Oct 2024, 1pm @ S4A Level 3 B & C Room Read More
  • NUS Admissions & Faculties Sharing for International Students

    16 November 2024, 11.20 am via Zoom (registration required) Read More
  • Venetoclax and azacitidine induce DFNA5-dependent cell death in leukemia

    19 September 2024, 1pm @ S4A Level 3 B & C Room Read More