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Single Cell Genome Sequence for DLP+ library A98181A
Dataset
EGAD00001009479
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Somatic pseudogenes acquired during cancer development – RNAseq
Dataset
EGAD00001000639
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Targeted RNA Expression Profiling via scTAMARA-seq
Dataset
EGAD00001015495
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Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90554B
Dataset
EGAD00001004731
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Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A75616C
Dataset
EGAD00001004726
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Papuan Genomes: high depth (30x) whole genome sequence data
Dataset
EGAD00001001634
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Whole-genome sequencing data for inflammatory breast cancer patients
Dataset
EGAD00001005749
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Stereotyped subset CLL RNA-seq from 100 patient with CLL
Dataset
EGAD00001009729
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Single Cell Genome Sequence for DLP+ library A96109A
Dataset
EGAD00001009452
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Transcriptomic origins of mpMRI visibility
Dataset
EGAD00001004397
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Whole Exome Sequencing
Dataset
EGAD00001004503
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TGL49 LFS sWGS
Dataset
EGAD00001010002
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Single Cell Genome Sequence for DLP+ library A118782A
Dataset
EGAD00001009435
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Transcriptomics sequencing 4 samples from the same KMT2A-rearranged Acute Lymphoblastic Leukemia patient
Dataset
EGAD00001009974
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There are 22 pairs of LAML cases in this project which belongs to LAML-CN. The library is constructed by the Illumina protocol.
Dataset
EGAD00001003317
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Somatic copy-number alterations in plasma circulating tumor DNA from advanced EGFR-mutated lung adenocarcinoma patients
Dataset
EGAD00001007505
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BLUEPRINT release January 2015, RNA-Seq for monocyte
Dataset
EGAD00001001191
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sn-RNAseq profiling of the impact of a cytokine storm model in human cardiac organoids
Dataset
EGAD00001007533
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RNA Seq Data
Dataset
EGAD00001001306
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Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90682
Dataset
EGAD00001004737
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Whole genome sequence data from Illumina HiSeqX instruments
Dataset
EGAD00001003562
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Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90689C
Dataset
EGAD00001004741
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sWGS data of Pap test smears and tumor tissues
Dataset
EGAD00001010141
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Latency and interval therapy affect the evolution in metastatic colorectal cancer
Dataset
EGAD00001005226
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Genotyping of GM samples
Dataset
EGAD00001010255