23093 results for "ega"

in 26.05 milliseconds.

• Targeted capture ctDNA Library CRCQV42Run021-18

  Targeted capture ctDNA Library CRCQV42Run021-18 from patient PBC0001653, plasma baseline sample

  Dataset EGAD00001010440

• Reference epigenome ADMSC04_smRNA-Seq data generated from KEP study

  A ADMSC04_smRNA-Seq single end data for adipose-derived mesenchymal stroaml cells

  Dataset EGAD00001003870

• HipSci - Bardet-Biedl Syndrome - Exome Sequencing - January 2016

  HipSci - Bardet-Biedl Syndrome - Exome Sequencing - January 2016

  Dataset EGAD00001001950

• Reference epigenome CKD27_C_Mesan_WGBS data generated from KEP study

  A CKD27_C_Mesan_WGBS paired end data for Mesangial cells(kidney)

  Dataset EGAD00001003471

• HipSci - Hereditary Cerebellar Ataxias - Exome Sequencing - July 2017

  HipSci - Hereditary Cerebellar Ataxias - Exome Sequencing - July 2017

  Dataset EGAD00001003521

• HipSci - Primary Immune Deficiency - Exome Sequencing - July 2017

  HipSci - Primary Immune Deficiency - Exome Sequencing - July 2017

  Dataset EGAD00001003526

• HipSci - Primary Immune Deficiency - RNA Sequencing - July 2017

  HipSci - Primary Immune Deficiency - RNA Sequencing - July 2017

  Dataset EGAD00001003536

• HipSci - Hereditary Spastic Paraplegia - RNA Sequencing - July 2017

  HipSci - Hereditary Spastic Paraplegia - RNA Sequencing - July 2017

  Dataset EGAD00001003537

• HipSci - Hereditary Cerebellar Ataxias - RNA Sequencing - July 2017

  HipSci - Hereditary Cerebellar Ataxias - RNA Sequencing - July 2017

  Dataset EGAD00001003538

• IfGH-10772

  Clinical and genetic information of an individual with RVOT-VT and a KCNK2 (TREK1) gene mutation obtained after whole exome sequencing.

  Dataset EGAD00001003328

• Reference epigenome CKD23_C_Mesan_WGBS data generated from KEP study

  A CKD23_C_Mesan_WGBS paired end data for Mesangial cells(kidney)

  Dataset EGAD00001003468

• Promoter capture HiC on KMS11 (multiple myeloma)

  Promoter capture HiC on KMS11 (multiple myeloma)

  Dataset EGAD00001003597

• PACA-CA Whole Genome Sequence bam files

  Merged bam files for PACA-CA Whole Genome Sequencing, for DCC release 27

  Dataset EGAD00001003927

• HipSci - Bardet-Biedl Syndrome - RNA Sequencing - January 2016

  HipSci - Bardet-Biedl Syndrome - RNA Sequencing - January 2016

  Dataset EGAD00001001954

• HipSci - Bardet-Biedl Syndrome - RNA Sequencing - April 2015

  HipSci - Bardet-Biedl Syndrome - RNA Sequencing - April 2015

  Dataset EGAD00001001952

• Patient 16CH

  One file of patient 16 with WGS done on Illumina HiSeq X-Ten. For research purpose and authorised user only.

  Dataset EGAD00001003440

• PACA-CA Whole Genome Sequence bam files

  Merged bam files for PACA-CA Whole Genome Sequencing, for DCC release 27

  Dataset EGAD00001003948

• UK10K_OBESITY_TWINSUK REL-2013-04-20

  UK10K_OBESITY_TWINSUK REL-2013-04-20

  Dataset EGAD00001000429

• RNA-Seq dataset

  10 RNA-Seq bam files including 4 cases with fusion and 6 controls without fusion.

  Dataset EGAD00001004360

• OT2_Illumina_WXS_MET

  Whole-exome sequencing on Illumina HiSeq2000/2500 of colorectal cancer metastasis sample (OT2_cohort)

  Dataset EGAD00001003379

• Illumina_WXS_T

  Whole-exome sequencing on Illumina HiSeq2000/2500 of colorectal cancer primary tumor sample

  Dataset EGAD00001002099

• HipSci - Bardet-Biedl Syndrome - Exome Sequencing - April 2015

  HipSci - Bardet-Biedl Syndrome - Exome Sequencing - April 2015

  Dataset EGAD00001001422

• HipSci - Hereditary Spastic Paraplegia - Exome Sequencing - July 2017

  HipSci - Hereditary Spastic Paraplegia - Exome Sequencing - July 2017

  Dataset EGAD00001003522

• THE MEDICAL RESEARCH COUNCIL – BRAIN BANK (MRC-BB) CONSORTIUM EXOME DATASET

  1461 Neuropathological and clinically characterised cases from the MRC Brain Bank

  Dataset EGAD00001001925

• DATA FILES FOR SJOS-WGS-2ndBatch

  DATA FILES FOR SJOS-WGS-2ndBatch

  Dataset EGAD00001001053

• Whole exome sequencing CHD trios

  Whole exome sequencing of families with Congenital Heart Defects (182 trios). Collaboration with David Brook, University of Nottingham.

  Dataset EGAD00001002200

• Nyamasati study

  Illumina whole genome sequencing to high depth (x50) of four Tanzanian individuals. Genomic DNA derived from peripheral whole blood.

  Dataset EGAD00001004370

• OT2_Illumina_WGS_T

  Whole-genome sequencing on Illumina HiSeq2000/2500 of colorectal cancer primary tumor sample (OT2_cohort)

  Dataset EGAD00001003375

• WGS data for MMML for Study EGAS00001002198

  Whole genome sequencing data for MMML (healthy cell_line)

  Dataset EGAD00001003283

• RNA-Seq and WXS from 6 glioblastoma patients

  RNA-Seq and WXS from 6 glioblastoma patients

  Dataset EGAD00001003293

• PACA-CA RNASeq bam files

  Bam files for PACA-CA RNA Seq analysis, for DCC release 27

  Dataset EGAD00001003945

• Spatial genomic heterogeneity in multiple myeloma

  Paired end Whole Exome Sequencing of fine-needle aspirates from 51 Mutliple Myeloma patients.

  Dataset EGAD00001003988

• SPTCL exome data

  Whole exome sequencing data of 17 SPTCL cases, including 7 matched-normal samples.

  Dataset EGAD00001004310

• The Ashkenazi Genome Consortium: Phase I

  Whole genome, high coverage, sequencing of 128 Ashkenazi Jewish controls

  Dataset EGAD00001000781

• Van Hippel-Lindau syndrome multi-region exome sequencing of two patients

  Van Hippel-Lindau syndrome multi-region exome sequencing of two patients

  Dataset EGAD00001000973

• FFPE Normal Panel V3 Cancer Panel

  FFPE normal panel generation for use with V3 cancer panel 0618521

  Dataset EGAD00001001122

• Cloning of the breakpoint of a novel translocation associated with T-acute lymphoblastic leukaemia

  Single case of T-ALL carrying t(4;6), a novel translocation.

  Dataset EGAD00001002193

• RNA-Seq files for SJOS study

  RNA-Seq files for SJOS study

  Dataset EGAD00001003154

• Targeted capture ctDNA Library CRCQV42Run022-13

  Targeted capture ctDNA Library CRCQV42Run022-13 from patient PBC0002826, plasma baseline sample

  Dataset EGAD00001010450

• Targeted capture ctDNA Library CRCQV42Run023-16

  Targeted capture ctDNA Library CRCQV42Run023-16 from patient PBC0002824, saliva sample

  Dataset EGAD00001010461

• Targeted capture ctDNA Library CRCQV42Run023-24

  Targeted capture ctDNA Library CRCQV42Run023-24 from patient PBC0002383, saliva sample

  Dataset EGAD00001010464

• Targeted capture ctDNA Library CRCQV42Run024-18

  Targeted capture ctDNA Library CRCQV42Run024-18 from patient PBC0001306, saliva sample

  Dataset EGAD00001010469

• Targeted capture ctDNA Library CRCQV42Run024-23

  Targeted capture ctDNA Library CRCQV42Run024-23 from patient PBC0003641, saliva sample

  Dataset EGAD00001010472

• Targeted capture ctDNA Library CRCQV42Run024-4

  Targeted capture ctDNA Library CRCQV42Run024-4 from patient PBC0001306, plasma baseline sample

  Dataset EGAD00001010473

• Targeted capture ctDNA Library CRCQV42Run025-14

  Targeted capture ctDNA Library CRCQV42Run025-14 from patient PBC0003385, saliva sample

  Dataset EGAD00001010480