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• Sequencing data for oesophageal and related samples - OACs release 6 (RNA)

  Dataset EGAD00001005375

• A96225C

  Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96225C 1034 samples; filetype=bam

  Dataset EGAD00001005355

• A96211C

  Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96211C 1397 samples; filetype=bam

  Dataset EGAD00001005354

• A96199B

  Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96199B 1170 samples; filetype=bam

  Dataset EGAD00001005353

• A96199A

  Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96199A 843 samples; filetype=bam

  Dataset EGAD00001005348

• A96193B

  Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96193B 2410 samples; filetype=bam

  Dataset EGAD00001005347

• A96226B

  Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96226B 1274 samples; filetype=bam

  Dataset EGAD00001005345

• A96172B

  Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96172B 1694 samples; filetype=bam

  Dataset EGAD00001005340

• A96146A

  Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96146A 1195 samples; filetype=bam

  Dataset EGAD00001005338

• Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data for library px0741_SA609X6

  55 samples; filetype=bam

  Dataset EGAD00001004822

• Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data for library px0740_SA609X6

  60 samples; filetype=bam

  Dataset EGAD00001004821

• Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data for library px0739_SA609X6

  52 samples; filetype=bam

  Dataset EGAD00001004820

• Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data for library px0738_SA609X6

  48 samples; filetype=bam

  Dataset EGAD00001004819

• Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data for library px0650_SA532X6

  71 samples; filetype=bam

  Dataset EGAD00001004818

• Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data for library px0544_SA532X6

  68 samples; filetype=bam

  Dataset EGAD00001004817

• Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data for library px0680_SA501X10A

  61 samples; filetype=bam

  Dataset EGAD00001004816

• Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data for library px0582_SA501X10A

  45 samples; filetype=bam

  Dataset EGAD00001004815

• Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data for library px0472_SA501X7A

  50 samples; filetype=bam

  Dataset EGAD00001004814

• Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data for library px0443_SA501X7A

  48 samples; filetype=bam

  Dataset EGAD00001004813

• Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data for library px0837_SA501X2

  40 samples; filetype=bam

  Dataset EGAD00001004812

• Sequencing data for oesophageal and related samples - Abujudeh et al (WGS, fastSeq)

  Data supporting: "Low-cost and clinically applicable copy number profiling using repeat DNA." Abujudeh et al. DNA WGS (BAM files) DNA fastSeq (fastq files) Tumours, Barrett's, normals.

  Dataset EGAD00001004289

• Clinical sequencing in multiple myeloma

  DNA (n=1281) and RNA (n=767) were extracted from bone marrow aspirates where CD138+ selection had been performed to enrich plasma cells from patients with monoclonal gammopathy of undetermined significance (MGUS), smoldering multiple myeloma (SMM), or multiple myeloma (MM). DNA and/or RNA were sent to Foundation Medicine where targeted sequencing was performed using their Foundation 1 Heme panel. Resulting BAM files were returned along with annotations for somatic events including single nucleotide mutations, indels and structural rearrangements.

  Dataset EGAD00001004113

• Sequencing data for oesophageal and related samples - Normals release 3 (RNA)

  Dataset EGAD00001003902

• Japanese liver cancer RNAseq

  RIKEN collection of RNA-seq reads for 458 liver cancer samples and matched normal liver from 247 donors.

  Dataset EGAD00001001880

• Sequencing data for oesophageal and related samples - Normals release 1 (RNA)

  Dataset EGAD00001002258