Prediction of type 2 diabetes using genome-wide polygenic risk score and metabolic profiles: A machine learning analysis of population-based 10-year prospective cohort study - eBioMedicine
Frontiers | A Study Protocol for Validation and Implementation of Whole- Genome and -Transcriptome Sequencing as a Comprehensive Precision Diagnostic Test in Acute Leukemias
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BMC Medical Genomics impact factor and citations:... | Exaly
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease | npj Genomic Medicine
Best practices in the real-world data life cycle | PLOS Digital Health
Impact of cancer mutational signatures on transcription factor motifs in the human genome
PDF) Within-pair differences of DNA methylation levels between monozygotic twins are different between male and female pairs
AI applications in functional genomics - ScienceDirect
Life | Free Full-Text | Artificial Intelligence and Cardiovascular Genetics
Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associ
Twelve quick steps for genome assembly and annotation in the classroom | PLOS Computational Biology
BMC Medical Genomics | Home page
Bioinformatics and Human Genomics Research - 1st Edition - Diego A. F
Single-nucleotide polymorphism - Wikipedia
Uncovering the impact of noncoding variants in neurodegenerative brain diseases: Trends in Genetics
Clinical providers' experiences with returning results from genomic sequencing: an interview study
Frontiers | Innovative in Silico Approaches for Characterization of Genes and Proteins
已确定删除SCI！1分+与2分+SCI合并值得投吗？ - 知乎
Journal Citation Reports JCR_2020 - Naresuan University Archive - Page 104 | Flip PDF Online | PubHTML5
The role of single-cell genomics in human genetics | Journal of Medical Genetics
Table 1 from Articles with short titles describing the results are cited more often | Semantic Scholar
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Genome-wide association study - Wikipedia
