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Accurate rare variant phasing of whole-genome and whole-exome sequencing data... diyicizhuce 2023-6-30 0537 diyicizhuce 2023-6-30 08:44
Imputation of low-coverage sequencing data from 150,119 UK Biobank genomes diyicizhuce 2023-6-30 0384 diyicizhuce 2023-6-30 08:40
Joint analysis of GWAS and multi-omics QTL summary statistics reveals a large... diyicizhuce 2023-6-20 0361 diyicizhuce 2023-6-20 09:11
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Annotating and prioritizing human non-coding variants with RegulomeDB diyicizhuce 2023-4-30 0268 diyicizhuce 2023-4-30 23:03
The ENCODE Imputation Challenge: a critical assessment of methods for cross-c... diyicizhuce 2023-4-19 0292 diyicizhuce 2023-4-19 23:08
Julia for biologists diyicizhuce 2023-4-11 0311 diyicizhuce 2023-4-11 14:20
XMAP: Cross-population fine-mapping by leveraging genetic diversity and accou... diyicizhuce 2023-4-3 0307 diyicizhuce 2023-4-3 19:36
GenoPipe: identifying the genotype of origin within (epi)genomic datasets diyicizhuce 2023-3-16 0383 diyicizhuce 2023-3-16 15:55
BridgePRS: A powerful trans-ancestry Polygenic Risk Score method diyicizhuce 2023-3-4 0312 diyicizhuce 2023-3-4 17:30
BioGPT: generative pre-trained transformer for biomedical text generation and... diyicizhuce 2023-2-25 0400 diyicizhuce 2023-2-25 14:55
Context-Aware Transcript Quantification from Long Read RNA-Seq data with Bambu diyicizhuce 2023-2-25 0378 diyicizhuce 2023-2-25 09:55
ChromDL: A Next-Generation Regulatory DNA Classifier diyicizhuce 2023-1-30 0396 diyicizhuce 2023-1-30 17:42
Size and composition of haplotype reference panels impact the accuracy of imp... diyicizhuce 2023-1-28 0432 diyicizhuce 2023-1-28 18:24
GeneDMRs: An R Package for Gene-Based Differentially Methylated Regions Analysis diyicizhuce 2022-8-4 11151 diyicizhuce 2022-8-4 21:16
Python hello world hsj003 2022-5-30 03061 hsj003 2022-5-30 03:50

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