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UnknownMutational Spectrum, Copy Number Changes, and Outcome: Results of a Sequencing Study of Patients With Newly Diagnosed Myeloma.
Not available
S-EPMC6485456 | biostudies-literature
GenomicsUK10K COHORT TWINSUK
The UK10K project proposes a series of complementary genetic approaches to find new low-frequency/rare variants contributing to disease phenotypes. These will be based on obtaining the genome-wide sequence of 4000 samples from the TwinsUK and ALSPAC cohorts (at 6x sequence coverage), and the exome ...
EGAS00001000108 | EGA
Genomicsuk10k_cohort_twins_rel_2011_12_01-sc-20120629 - samples
UK10K_COHORT_TWINS REL-2011-12-01
EGAD00001000194 | EGA
Genomicsuk10k_cohort_imputation_rel_2012_06_02-sc-20140306 - samples
UK10K_COHORT_IMPUTATION REL-2012-06-02: imputation reference panel (20140306); Merged UK10K+1000Genomes Phase 3 imputation reference panel added (20160420)
EGAD00001000776 | EGA
Genomicsuk10k_cohort_twinsuk_rel_2012_06_02-sc-20131101-phenotypes - samples
UK10K_COHORT_TWINSUK REL-2012-06-02: Phenotype data
EGAD00001000790 | EGA
Genomicsuk10k_cohort_alspac_rel_2012_06_02-sc-20131101-phenotypes - samples
UK10K_COHORT_ALSPAC REL-2012-06-02: Phenotype data
EGAD00001000789 | EGA
Genomicsuk10k_cohort_twinsuk_rel_2012_06_02-sc-20131101 - samples
UK10K_COHORT_TWINSUK REL-2012-06-02: Low-coverage whole genome sequencing; variant calling, genotype calling and phasing
EGAD00001000741 | EGA
GenomicsHELIC_MANOLIS_OmniExpress - samples
Samples from the Greek island of Crete, MANOLIS cohort
EGAD00010000522 | EGA
GenomicsIllumina Human OmniExpress genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Isolated populations can empower the identification of rare variation associated with complex traits through next generation association studies. Here we have genotyped individuals from a Greek population isolate on the Illumina Human OmniExpress BeadChip array. The HELIC (Hellenic Isolated Cohorts)...
EGAS00001000687 | EGA
GenomicsMassive Genomic Rearrangment Acquired in a Single Catastrophic Event During Cancer Development
Cancer is driven by mutation. Using Agilent exome hybridisation capture and Illumina GA massively parallel sequencing technology, we aim to sequence ~1600 microRNAs plus the protein coding genome of 25 matched human renal cancer samples. Bespoke algorithms are being developed to identify the somatic...
EGAS00000000029 | EGA
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