Supplementary Tables S1-S12 from Gene-Level Germline Contributions to Clinical Risk of Recurrence Scores in Black and White Patients with Breast Cancer
Annotated .maf somatic mutation data files for 30 tumour samples from 22 patients Method for somatic mutation calling Somatic single nucleotide variants (SNVs), insertions and deletions (InDel
BackgroundEchinoderm microtubule-associated protein-like 4 (EML4) is the canonical anaplastic lymphoma kinase (ALK) fusion partner in non-small cell lung cancer (NSCLC), and ALK-positive patients show
Through RNA-sequencing in Leiomyoma with bizarre nuclear and corresponded normal myometrium, we can get the significantly different expressed genes in Leiomyoma with bizarre nuclear, and at the same t
Sequence data in fastq format was aligned to the GRCh38 reference genome with BWA-MEM and preprocessed with GATK for indel realignment and base quality score recalibration. Aligned sequence was analyz