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152: One-Well Multiplex ddPCR for Hereditary Alpha Tryptasemia	Base by Base	16:53
151: EQA of ctDNA Mutation Testing Across the COIN Consortium	Base by Base	16:21
150: Patrilineal segmentary systems and the post‑Neolithic Y‑chromosome bottleneck	Base by Base	17:52
149: Cultural Hitchhiking and the Post‑Neolithic Y‑Chromosome Bottleneck	Base by Base	15:04
148: Systematic Minigene-Based Splicing Analysis and Tentative Clinical Classification of 52 CHEK2 Splice-Site Variants	Base by Base	14:44
147: Comprehensive Annotation of Complete ABO Alleles and Resolution of ABO Variants	Base by Base	15:37
146: Automated and Decentralized Genomic Profiling of Plasma Cell-Free DNA in Solid Tumors	Base by Base	15:56
145: A Validated Highly Sensitive Microsatellite Instability Assay Identifies PMS2 Variants in CMMRD	Base by Base	16:59
144: Revised time estimation of the ancestral human chromosome 2 fusion	Base by Base	17:10
143: The genetic history of the Southern Caucasus: 5,000 years of continuity despite high mobility	Base by Base	18:56
142: Specifications of the ACMG/AMP Guidelines for PALB2 Variant Interpretation	Base by Base	16:35
141: RetiGene, a comprehensive gene atlas for inherited retinal diseases	Base by Base	26:12
140: Landscapes of missense variant impact for human superoxide dismutase 1	Base by Base	20:18
139: MosCoverY: A new method to estimate mosaic loss of Y chromosome from sequencing coverage data	Base by Base	14:03
138: Social exposome and brain health outcomes of dementia across Latin America	Base by Base	19:43
137: Rethinking RNA-binding proteins: Riboregulation challenges prevailing views	Base by Base	25:11
136: Gene Context Drift Identifies Drug Targets to Mitigate Cancer Treatment Resistance	Base by Base	14:48
135: Global impact of micronutrients in modern human evolution	Base by Base	14:26
134: Single-Cell Maps Link Intestinal Metaplasia to Esophageal Adenocarcinoma Risk	Base by Base	15:47
133: Culture-Independent Meta‑Pangenomics Reveals Gut Genome Links to Child Growth	Base by Base	24:31
132: Tumor transcriptome classifiers predict treatment sensitivity in advanced prostate cancer	Base by Base	20:35
131: pBI143: The Human Gut’s Hidden Heavyweight	Base by Base	17:59
130: Combining Evidence from Human Genetic and Functional Screens to Identify Pathways Altering Obesity and Fat Distribution	Base by Base	20:24
129: Structural variation and diversification of the NPIP gene family from the human pangenome	Base by Base	22:11
128: LINE‑1 Promoters Orchestrate Early Human Brain Development	Base by Base	15:26
127: In silico generation of synthetic cancer genomes using generative AI	Base by Base	17:36
126: Molecular and developmental deficits in Smith-Magenis syndrome human stem cell-derived cortical neural models	Base by Base	20:59
125: Tackling a disease on a global scale, the Global Parkinson’s Genetics Program, GP2: A new generation of opportunities	Base by Base	22:46
124: Exploring the Omnigenic Architecture of Selected Complex Traits	Base by Base	23:47
123: Dominant‑Negative ATP5F1A Variants Uncouple Complex V and Drive Neurological Disease	Base by Base	18:12
122: Patient Stratification Reveals the Molecular Basis of Disease Co-Occurrences	Base by Base	19:57
121: G-quadruplexes as a Source of Vulnerability in BRCA2-deficient Granule Cell Progenitors and Medulloblastoma	Base by Base	19:02
120: Rare BMAL1 Variants Link the Circadian Clock to Neurodevelopment	Base by Base	22:30
119: G‑Quadruplex Stabilization Triggers Pericentromeric DNA Breaks in B Cells	Base by Base	18:35
118: Cancer cells subvert the primate-specific KRAB zinc finger protein ZNF93 to control APOBEC3B	Base by Base	19:11
117: Pol III–linked polyadenylation fuels SINE RNA accumulation during infection	Base by Base	16:00
116: Cell Type–Specific Purifying Selection of Synonymous mtDNA Variation	Base by Base	15:53
115: A Transcriptomic, Proteomic, and Functional Genetic Atlas Dissects Neurofibromin Function in the Peripheral Nervous System	Base by Base	15:24
114: One-hour extraction-free loop-mediated isothermal amplification HPV DNA assay for point-of-care testing in Maputo, Mozambique	Base by Base	16:31
113: Joint, Multifaceted Genomic Analysis Enables Diagnosis of Ultra-Rare Monogenic Presentations	Base by Base	22:08

152: One-Well Multiplex ddPCR for Hereditary Alpha Tryptasemia

Base by Base

16:53

151: EQA of ctDNA Mutation Testing Across the COIN Consortium

Base by Base

16:21

150: Patrilineal segmentary systems and the post‑Neolithic Y‑chromosome bottleneck

Base by Base

17:52

149: Cultural Hitchhiking and the Post‑Neolithic Y‑Chromosome Bottleneck

Base by Base

15:04