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331: Bi-allelic NDUFA5 variants and complex I mitochondriopathy	Base by Base	26:50
330: 5ULTRA: Mapping 5′ UTR variants that alter protein translation	Base by Base	22:56
329: Large future genetic diversity losses predicted despite habitat protection	Base by Base	22:16
328: Variant selection boosts R2 for haptoglobin (HP) in cis‑Mendelian randomization	Base by Base	23:39
327: Bi-allelic ATG12 variants impair ATG12-ATG5 conjugation, LC3 lipidation and neural development	Base by Base	19:17
326: DUO-1 protects REC-8 cohesin and synaptonemal complex stability in Caenorhabditis elegans meiosis	Base by Base	24:34
325: cis-pcQTL mapping reveals allelic proxitropy across neighboring human genes	Base by Base	23:57
324: ZSWIM8–CUL3 clamp on AGO2–miR-7 reveals mechanism of targeted microRNA degradation	Base by Base	20:16
323: Meat consumption and APOE ε3/ε4–ε4/ε4: slower cognitive decline and lower dementia risk in SNAC‑K	Base by Base	20:16
322: Bi-allelic RNU6ATAC and RNU4ATAC variants cause infancy-onset autoimmune diabetes via minor spliceosome U12 intron retention	Base by Base	22:50
321: All five canonical nucleobases detected in Ryugu samples	Base by Base	29:52
320: Sex-stratified cQTL mapping identifies TOX (IFN-γ) and EGFR (IL-10) regulators in Dutch and Tanzanian cohorts	Base by Base	23:15
319: Predicting reduced-penetrance TP53 variants from functional assays and random forest models	Base by Base	23:35
318: RNU6ATAC variants cause U6atac-driven minor spliceopathy with transcriptome-wide minor intron retention	Base by Base	21:30
317: COPD sQTL colocalization in lung and blood identifies FBXO38 and BTC splicing mechanisms	Base by Base	21:10
316: Inclusion bias in UCLA ATLAS: enrollment models, weighting, and effects on GWAS and PGS	Base by Base	23:18
315: PLE11-encoded Rta restricts ICP1 tail assembly in Vibrio cholerae outbreaks	Base by Base	23:59
314: Proactive Genomic Reanalysis at Boston Children’s: VS-NN, HPO NLP and DRAGEN find diagnoses in pediatric ES/GS	Base by Base	22:41
313: Integrating Polygenic Risk Scores and Social Determinants of Health across Populations	Base by Base	24:46
312: Mfsd2a transports LPC to maintain epidermal linoleate pools and desquamation	Base by Base	14:53
311: mtG3PDH (GPO1) loss in Drosophila impairs mitochondrial ATP/O, O2 consumption, and ROS	Base by Base	42:24
310: Infant gut microbiota restoration — maternal FMT, Bifidobacterium and Bacteroides recovery after C‑section	Base by Base	49:10
309: LASI-DAD 2,680-sample WGS panel boosts LD maps, imputation, and PRS in Indian genomes	Base by Base	23:42
308: PANDORA-seq reveals conserved rsRNA length shift and tsRNA/rsRNA aging cliff in mouse and human sperm	Base by Base	22:25
307: SNIPE membrane nuclease cleaves phage λ DNA during ManYZ-mediated genome injection in Escherichia coli	Base by Base	27:44
306: SAXO6 loss-of-function in photoreceptor cilia links a microtubule inner protein to late-onset retinal dystrophy	Base by Base	25:09
305: Human cis-regulatory variants dissected by MPRA at single-nucleotide resolution	Base by Base	22:24
304: Patrilineal Y‑chromosome drive in a Utah pedigree (67% male offspring)	Base by Base	18:13
303: Short-read sequencing and genome skimming for biodiversity monitoring and phylogenomics	Base by Base	29:00
302 auf Deutsch: SMN1/SMN2-Spleißen und Mechanismen im letzten Exon — Hommage an Brunhilde Wirth	Base by Base	13:58
302: SMN1/SMN2 splicing and last-exon mechanisms — Tribute to Brunhilde Wirth	Base by Base	24:12
301: Biobank Mendelian randomization prioritizes 6,447 genes and nominates ANXA2 for dyslipidemia	Base by Base	20:53
300: Population-scale WGS links MHC class II antigen presentation to persistent Epstein–Barr virus (EBV) DNA	Base by Base	21:48
299: UFM1 loss and R81C mutation disrupt neuronal translation, ER stress, and synaptogenesis	Base by Base	21:15
298: Bi-allelic FSD1L variants in retinitis pigmentosa implicate photoreceptor axoneme	Base by Base	20:16
297: Bi-allelic FSD1L variants disrupt mitotic spindle and ciliogenesis in an L1-like neurodevelopmental disorder	Base by Base	21:27
296: snaR-A ncRNA antagonizes U2 snRNP SF3B2 to drive intron retention in human cells	Base by Base	20:38
295: CFTR deltaF508 and CF-risk variants protect against IBD in large exome study	Base by Base	28:25
294: Alternative splicing, exonization and lineage-specific isoforms: PTBP1, MAPT and TE-derived exons in mammalian evolution	Base by Base	36:58
293: IndeLLM (ESM2) zero-shot scoring and Siamese transfer learning for in-frame indel prediction (MCC 0.77)	Base by Base	17:53

331: Bi-allelic NDUFA5 variants and complex I mitochondriopathy

Base by Base

26:50

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

Base by Base

22:56

329: Large future genetic diversity losses predicted despite habitat protection

Base by Base

22:16

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

Base by Base

23:39