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Whole-Exome Sequencing Analysis of Tumor Biopsies from a Colorectal Cancer Patient

After the sequencing, reads were aligned against the reference human genome GRCh38 using Burrows-Wheeler Aligner (BWA, v0.7.12). SNVs and indels were called using MuTect2 (GATK 4.1.4.1). SNVs or indels with a VAF < 5% or those that were covered by fewer than three reads were discarded., iIf the SNVs were found in both components of one sample, a cut-off of two reads was applied. We further excluded variants identified in at least two of a panel of 210 non-tumor samples, including the non-tumor samples included in the current study. Variant annotation was performed by SnpEff software v.4.1.

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Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID Study Title Study Type
EGAS50000001385 Whole Genome Sequencing

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Quality Report
Located in
EGAF50000486302 bam 17.5 GB
EGAF50000486303 bam 13.7 GB
EGAF50000486304 bam 17.3 GB
EGAF50000486305 bam 16.9 GB
EGAF50000486306 bam 18.0 GB
EGAF50000486307 xlsx 490.6 kB
6 Files (83.5 GB)