Schedule of NCBI Activities
Wednesday, November 6 (all times are in MT)
9:30 a.m. - 4:30 p.m. |
Exhibit Hall Booth #1021 |
NCBI Exhibit Booth Meet the Experts Sessions 11:00 a.m - 12:00 p.m. Adam Stine, MS Sequence Read Archive (SRA) 12:00 p.m - 1:00 p.m. Adriana Malheiro, MS, LCGC MedGen, GTR, and MGS 1:00 p.m. - 2:00 p.m. Minghong Ward, MS dbGaP FHIR API 2:00 p.m. - 3:00 p.m. Chunlin Xiao, PhD Somatic Mutation Benchmark 3:00 p.m. - 4:00 p.m. Melissa Landrum, PhD ClinVar |
2:30 p.m. - 4:30 p.m. |
Session: Genetic, Genomic, and Epigenomic Resources and Databases Poster Wednesday Session Room: Exhibit & Poster Hall F |
Adriana Malheiro, MS, LCGC Brandi Kattman, MS/MS, CGC #1078W: MedGen at NCBI: Empowering Biomedical Discovery and Clinical Care by Integrating Multiple Ontologies |
2:30 p.m. - 4:30 p.m. |
Session: Genetic, Genomic, and Epigenomic Resources and Databases Poster Wednesday Session Room: Exhibit & Poster Hall F |
Vinita Joardar, PhD #1076W: Matched Annotation from NCBI and EMBL-EBI (MANE): Current Status, Stability and Future Plans for expansion of the MANE dataset |
Thursday, November 7 (all times are in MT)
9:30 a.m. - 4:30 p.m. |
Exhibit Hall Booth #1021 |
NCBI Exhibit Booth Meet the Experts Sessions 10:00 a.m. - 11:00 a.m. Minghong Ward, MS dbGaP FHIR API 11:00 a.m - 12:00 p.m. Adam Stine, MS Sequence Read Archive (SRA) 12:00 p.m - 1:00 p.m. Chunlin Xiao, PhD Somatic Mutation Benchmark 1:00 p.m. - 2:00 p.m. Brandi Kattman, HS/MS, CGC Clinical Genetics Resources 2:00 p.m. - 3:00 p.m. Vinita Joardar, PhD RefSeq 3:00 p.m. - 4:00 p.m. Melissa Landrum, PhD ClinVar |
2:30 p.m. - 4:30 p.m. |
Session: Genetic, Genomic, and Epigenomic Resources and Databases Poster Room: Exhibit & Poster Hall F |
Valerie Schneider, PhD #1091T: The NIH Comparative Genomics Resource (CGR): Maximizing the impact of research organisms to human health |
2:30 p.m. - 4:30 p.m. |
Session: Cancer Poster Thursday Session Room: Exhibit & Poster Hall F |
Chunlin Xiao, PhD #8029T: Haplotype-resolved assemblies for somatic mutation benchmark development for a GIAB tumor-normal pair reference sample |
Friday, November 8 (all times are in MT)
9:30 a.m. - 4:30 p.m. |
Exhibit Hall Booth #1021 |
NCBI Exhibit Booth Meet the Experts Sessions 11:00 a.m - 1:00 p.m. Valerie Schneider, PhD Comparative Genomics Resource (CGR) 1:00 p.m. - 2:00 p.m. Brandi Kattman, HS/MS, CGC Medical Genetics & Human Variation 2:00 p.m. - 3:00 p.m. Vinita Joardar, PhD RefSeq 3:00 p.m. - 4:00 p.m. Adriana Malheiro, MS, LCGC MedGen, GTR, and MGS |
8:30 a.m. - 8:45 a.m. |
Session: How do we describe and ascribe clinical significance to the non-coding genome? Room: Mile High Ballroom 2 & 3 |
Melissa Landrum, PhD Featured Symposium Talk How do we represent functional effects of non-coding variants in public databases? |
2:30 p.m. - 4:30 p.m. |
Session: Omics Technologies Poster Friday Session Room: Exhibit & Poster Hall F |
Adam Stine, MS #1172F: Speeding up Genetic Analysis with a Smaller Data Format |
2:30 p.m. - 4:30 p.m. |
Session: Genetic, Genomic, and Epigenomic Resources and Databases Poster Friday Session |
Minghong Ward, MS #1062F: Empower Users with Programmatic Access to dbGaP Data Using FHIR |
Last Reviewed: October 22, 2024