Base by Base

Base by Base

Base by Base explores advances in genetics and genomics, with a focus on gene-disease associations, variant interpretation, protein structure, and insights from exome and genome sequencing. Each episode breaks down key studies and their clinical relevance—one base at a time. Powered by AI, Base by Base offers a new way to learn on the go. Special thanks to authors who publish under CC BY 4.0, making open-access science faster to share and easier to explore.

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Avsnitt(440)

8: A structural variation reference for medical and population genetics

8: A structural variation reference for medical and population genetics

Collins RL et al et al., Nature - This episode reviews gnomAD-SV, a sequence-resolved reference of structural variants from 14,891 genomes that catalogs 433,371 SVs (335,470 high-quality) and integrat...

17 Apr 202524min

7: Using high-resolution variant frequencies to empower clinical genome interpretation

7: Using high-resolution variant frequencies to empower clinical genome interpretation

Whiffin N et al., Genetics in Medicine - A statistical framework uses large reference allele-frequency data (ExAC) together with disease prevalence, heterogeneity, penetrance, and sampling variance to...

17 Apr 202519min

6: TRMT1, tRNA m2,2G, and Intellectual Disability

6: TRMT1, tRNA m2,2G, and Intellectual Disability

Efthymiou S et al., The American Journal of Human Genetics - A global cohort study identifies bi-allelic TRMT1 variants that cause developmental delay and intellectual disability, links those variants...

17 Apr 202526min

5: Promoter Footprints Predicting Preterm Birth

5: Promoter Footprints Predicting Preterm Birth

Guo Z et al., PLOS Medicine - Large multi-center case-control study shows promoter-region nucleosome footprints in plasma cell-free DNA can predict spontaneous preterm birth. The authors developed PTe...

16 Apr 202514min

4: How CXCL12 Shapes Coronary Dominance

4: How CXCL12 Shapes Coronary Dominance

Rios Coronado PE et al., Cell - A multi-ancestry GWAS in >61,000 veterans identifies CXCL12 as a top locus influencing whether the right or left coronary tree supplies the posterior heart; fetal expre...

16 Apr 202517min

3: Data-driven heuristics for splice-altering variants

3: Data-driven heuristics for splice-altering variants

Sullivan P et al., The American Journal of Human Genetics - A concise walkthrough of data-driven heuristics and a splicing checklist derived from large-scale exon, branchpoint, and experimentally vali...

16 Apr 202522min

2: Tube additives and cfDNA integrity: why EDTA still leads

2: Tube additives and cfDNA integrity: why EDTA still leads

Barra G et al., LabMed (2025) 2, 4 - A comparative study of blood collection tubes (EDTA, citrate, heparin, serum) from 15 healthy volunteers showing how anticoagulants affect baseline cell-free DNA, ...

16 Apr 202516min

1: Structure-Informed Computational Evidence Sharpens BRCA1 Missense Classification

1: Structure-Informed Computational Evidence Sharpens BRCA1 Missense Classification

Ramadane-Morchadi L et al., The American Journal of Human Genetics - This episode reviews a study that evaluates how structure-based computational scores (AlphaMissense, FoldX DDG using PDB or AlphaFo...

15 Apr 202520min

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