23227 results for "ega"

in 35.40 milliseconds.

• Feasibility of targeted capture sequencing in FFPE cancer specimens 2

  Testing the feasibility of genome-scale sequencing in routinely collected formalin-fixed paraffin-embedded (FFPE) cancer specimens versus matched fresh-frozen samples using targeted pulldown capture prior to Illumina sequencing.

  Dataset EGAD00001001448

• Whole Exome Sequencing (WES) for St. Jude High Grade Glioma (HGG) study

  Whole Exome Sequencing (WES) for St. Jude High Grade Glioma (HGG) study

  Dataset EGAD00001000807

• Single Cell Genome Sequence for DLP+ library A98240A

  Single Cell Genome Sequence for triple negative breast cancer patient-derived xenograft SA530 passage 3 on DLP+ library A98240A

  Dataset EGAD00001009480

• RaCHseq data

  Captured single-cell long-read data of a cohort of CLL patients receiving VEN treatment for resistance study

  Dataset EGAD00001008365

• Single Cell Genome Sequence for DLP+ library A96190B

  Single Cell Genome Sequence for high grade serous ovarian carcinoma patient-derived xenograft SA1051A passage 1 on DLP+ library A96190B

  Dataset EGAD00001009466

• Single Cell Genome Sequence for DLP+ library A96207B

  Single Cell Genome Sequence for high grade serous ovarian carcinoma patient-derived xenograft SA1052B passage 1 on DLP+ library A96207B

  Dataset EGAD00001009474

• Differential Presence of Exons in Cell-Free DNA

  Differential Presence of Exons in Cell-Free DNA Reveals Different Patterns in Colorectal Cancer Between Metastatic, Non-Metastatic Patients and Healthy Donors. 159 samples, Illumina sequencing technology.

  Dataset EGAD00001009510

• LifeLines-DEEP Gut MGS

  Meta-genomic sequencing of 1,200 LifeLines-DEEP participants

  Dataset EGAD00001001991

• Genetic landscape of Extranodal NK/T-cell lymphoma

  Whole-exome sequence (WES) data of tumor-normal pairs from 40 ENKTCL patients and RNA sequence (RNA-seq) data of tumors from 20 ENKTCL patients.

  Dataset EGAD00001009852

• sWGS of cfDNA from metastatic CRC patients

  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.

  Dataset EGAD00001010293