Base by Base
Total duration:
11 h 54 min
170: Maternal Age, Meiotic Recombination Failure, and Triploidy in Humans
Base by Base
17:03
169: Deep mutational scanning of the insulin receptor guides precision therapy for insulin resistance
Base by Base
21:13
168: Low circulating miR-190a-5p predicts progression of chronic kidney disease
Base by Base
19:10
167: DeepScence: Detecting Senescent Cells at Single-Cell and Spatial Resolution
Base by Base
21:40
166: Molecular Squeezing: How Coronin, Cofilin, and AIP1 Rapidly Disassemble Actin Filaments
Base by Base
13:37
165: Protist Genomics: Key to Understanding Eukaryotic Evolution
Base by Base
19:24
164: m6A in the coding sequence: linking deposition, translation, and decay
Base by Base
14:46
163: Animal origins: looping back in time
Base by Base
14:18
162: Spatially Resolved microRNA Expression in Tissues: Technologies, Challenges, and Opportunities
Base by Base
20:15
161: Decoding Genomic Landscapes of Introgression
Base by Base
20:55
160: The Long‑Read Leap in Single‑Cell Omics
Base by Base
15:36
159: The Untapped Potential of Short‑Read Sequencing in Biodiversity Research
Base by Base
15:56
158: Interruptions in Repeat Expansion Diseases: How Are They Gained and Lost?
Base by Base
22:35
157: Synthetic gametes and the non-identity problem: the babies of tomorrow
Base by Base
14:32
156: RAEFISH: Sequencing-free whole-genome spatial transcriptomics at single-molecule resolution
Base by Base
17:07
155: EIF3A/EIF3B Loss-of-Function: A Cardiocraniofacial Neurodevelopmental Syndrome
Base by Base
15:53
154: Multiple-testing corrections in selection scans using identity-by-descent segments
Base by Base
20:05
153: Skeletal muscle eQTL meta-analysis implicates genes in the genetic architecture of muscular and cardiometabolic traits
Base by Base
15:13
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
