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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Episoder(441)

334: LINE-1 Recombination with Diverse RNAs

334: LINE-1 Recombination with Diverse RNAs

Law C-T et al., Cell Genomics - Law and Burns introduce TiMEstamp, a comparative-genomics pipeline that dates LINE-1 insertions from multiple sequence alignments and discovers hundreds of LINE-1 chime...

5 Apr 21min

333: Holistic determination of cfDNA ends

333: Holistic determination of cfDNA ends

Jiang P et al., Cell Genomics - This episode reviews a Cell Genomics study that uses ssDNA '2-end' and novel '4-end' sequencing to profile native 5′ and 3′ termini of plasma cfDNA. The work identifies...

4 Apr 24min

333: Holistic determination of cfDNA ends

333: Holistic determination of cfDNA ends

Jiang P et al., Cell Genomics - This episode reviews a Cell Genomics study that uses ssDNA '2-end' and novel '4-end' sequencing to profile native 5′ and 3′ termini of plasma cfDNA. The work identifies...

4 Apr 0s

332: When Chromatin Filters Force: Age, AP-1, and Fibroblast Mechanotransduction

332: When Chromatin Filters Force: Age, AP-1, and Fibroblast Mechanotransduction

Liao Y et al., PNAS - Human dermal fibroblasts from young and old donors were embedded in 3D collagen and exposed to mechanical tension and TGF-β. Combining bulk RNA‑seq, ATAC‑seq, imaging, and pertur...

2 Apr 22min

331: Bi-allelic NDUFA5 variants and complex I mitochondriopathy

331: Bi-allelic NDUFA5 variants and complex I mitochondriopathy

Tan et al et al., The American Journal of Human Genetics - This report identifies bi-allelic NDUFA5 variants in four individuals from three families causing an isolated mitochondrial complex I deficie...

31 Mar 26min

330: 5ULTRA: Mapping 5′ UTR variants that alter protein translation

330: 5ULTRA: Mapping 5′ UTR variants that alter protein translation

Chaldebas M et al., The American Journal of Human Genetics - Chaldebas et al. present 5ULTRA, a computational pipeline that integrates uORF databases, Kozak-motif features, splicing prediction, and a ...

30 Mar 22min

329: Large future genetic diversity losses predicted despite habitat protection

329: Large future genetic diversity losses predicted despite habitat protection

Mualim KS et al., Proceedings of the National Academy of Sciences - This study develops spatiotemporal population-genetic models calibrated with genomic data to predict how habitat loss and fragmentat...

30 Mar 22min

328: Variant selection boosts R2 for haptoglobin (HP) in cis‑Mendelian randomization

328: Variant selection boosts R2 for haptoglobin (HP) in cis‑Mendelian randomization

Zhou A et al., Human Genetics and Genomics Advances - Comparing LD‑pruning, COJO, SuSiE and PCA in haptoglobin (HP) cis‑region data, the study finds including non‑lead variants substantially increases...

27 Mar 23min

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