Need Help?

Liquid Biopsy Data Access Committee

Contact Information

Ellen Heitzer
ellen.heitzer@medunigraz.at

Request Access

This DAC controls 7 datasets

Dataset ID	Description	Technology	Samples
EGAD00001007930	Mutation analysis of 77 frequently mutated genes in NSCLC in plasma DNA and corresponding PBMCs of NSCLC patients under ICI using the AVENIO Expanded Kit.	Illumina HiSeq 4000 NextSeq 550	516
EGAD00001008396	Targeted next-generation sequencing (NGS) of 93 frequently mutated genes in breast cancer using the QIAseq Human Breast Cancer Targeted Panel (QIAGEN), which uses digital sequencing by incorporating unique molecular barcodes (UMI).	Illumina MiSeq NextSeq 550	187
EGAD00001008397	Paired end shallow whole genome sequencing (sWGS) data for the identification of genomewide somatic copy number alterations (SCNA) and the estimation of tumor fractions.	NextSeq 550	185
EGAD00001009110	Extracted regions from WGS of Ewing sarcoma spanning fusion breakpoints +/- 100kb for ctDNA tracking in plasma	Illumina NovaSeq 6000	1
EGAD00001010100	These are aligned paired-end reads from Illumina NovaSeq 6000 whole-genome sequencing of 4 cfDNA samples extracted from blood plasma (plasma-Seq). Three samples from patients with breast cancer, prostate cancer, or colorectal cancer and one sample from a healthy individual were aligned to GRCh38 (GCA_000001405.15_GRCh38_no_alt_plus_hs38d1_analysis_set). The observed GC bias is different in each of these cfDNA samples which leads to different average GC content per sample. This bias is corrected using the GCparagon commandline tool.	Illumina NovaSeq 6000	2
EGAD00001010293	Paired end shallow whole genome sequencing (sWGS) data (FASTQ) for the identification of genomewide somatic copy number alterations (SCNA) and the estimation of tumor fractions.		30
EGAD00001010294	Aligned NGS data (BAM) of 77 frequently mutated genes in cancer using the AVENIO Expanded platform.		30