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Additional file 3: Table S1. of Application of single-cell RNA sequencing in optimizing a combinatorial therapeutic strategy in metastatic renal cell carcinoma

Year: 2016

Type: dataset

Abstract: Somatic mutations identified in tumor samples from whole-exome sequencing. Single-nucleotide variants (SNVs) were annotated by implementing SnpEff. Whole-exome sequencing data of paired patient blood was used to identify somatic variants in parental tumors and matched xenografts of pRCCs and mRCCs, which are shown in separate sheets. (XLSX 218 kb)

Source: Figshare

DOI: 10.6084/m9.figshare.c.3613934_d6

Authors: Kyu-Tae Kim, Lee, Hye, Hae-Ock Lee, Song, Hye, Jeong, Da, Shin, Sang, Hyunho Kim, Yoojin Shin, Do-Hyun Nam, Jeong, Byong, Kirsch, David, Joo, Kyeung, Woong-Yang Park

Language: English

Topic: Renal cell carcinoma treatment

Subfield: Pulmonary and Respiratory Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: green

OpenAlex ID: W4394535302

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