专题:Genomics and Rare Diseases

This cluster of papers focuses on the standards, guidelines, and tools for interpreting genetic variants, particularly in the context of clinical genomics and Mendelian disorders. It includes topics such as pathogenicity prediction, functional annotations, sequence interpretation, and the use of exome sequencing for identifying disease-causing variants.
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FinnGen provides genetic insights from a well-phenotyped isolated population

article Full Text OpenAlex 4207 FWCI627.4091

Accurate proteome-wide missense variant effect prediction with AlphaMissense

article Full Text OpenAlex 2123 FWCI310.1471

A genomic mutational constraint map using variation in 76,156 human genomes

article Full Text OpenAlex 1711 FWCI248.1468

Next-Generation Sequencing Technology: Current Trends and Advancements

article Full Text OpenAlex 1288 FWCI95.5396

Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee

article Full Text OpenAlex 1162 FWCI77.4265

High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

article Full Text OpenAlex 1088 FWCI112.6402

Rare coding variants in ten genes confer substantial risk for schizophrenia

article Full Text OpenAlex 976 FWCI111.3583

Genomic data in the All of Us Research Program

article Full Text OpenAlex 823 FWCI195.326

Nucleotide Transformer: building and evaluating robust foundation models for human genomics

article Full Text OpenAlex 660 FWCI74.3841

Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria

article Full Text OpenAlex 580 FWCI56.0513