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525 results for "retinitis+pigmentosa+2017+surgery+blog+"my+twin+died+at+birth""

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blog dac dataset documentation study

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cancer genomics case set case-control clinical cohort clinical trial cohort collection control set copy number variation (cnv) cross-sectional epigenetics exome sequencing family gene regulation study interventional longitudinal longitudinal cohort metagenomics multiplex families nested case-control observational other parent-offspring prospective randomized controlled clinical trial rna sequencing rnaseq single cell analysis transcriptome analysis transcriptome sequencing tumor tumor vs. matched-normal whole genome sequencing

Dataset types

amplicon sequencing chip-seq chromatin accessibility profiling by high-throughput sequencing exome sequencing genotyping by array histone modification profiling by high-throughput sequencing methylation binding domain sequencing methylation profiling by high-throughput sequencing phenotype information transcriptome profiling by high-throughput sequencing whole genome sequencing

Dataset technologies

complete genomics hiseq x ten illumina illumina genome analyzer ii illumina genome analyzer iix illumina hiscansq illumina hiseq 2000 illumina hiseq 2500 illumina hiseq 3000 illumina hiseq 4000 illumina methylationepic array illumina miseq illumina novaseq 6000 illumina novaseq x infinium methylationepic beadchip infinium methylationepic v2.0 beadchip ion genestudio s5 ion torrent proton minion nanostring technology nextseq 2000 nextseq 500 nextseq 550 sequel unspecified

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[CL:0000057] [CL:0000236] [CL:0000842] [CL:2000006] [DOID:0050756] [EFO:0000174] [EFO:0000503] [EFO:0000540] [EFO:0004905] [EFO:0005803] [EFO:1000042] [HP:0001258] [NCIT:C0549184] [NCIT:C115935] [NCIT:C27204] [NCIT:C2952] [Orphanet:110] [Orphanet:183518] [Orphanet:217569] [Orphanet:2322] [Orphanet:3095] [Orphanet:552] [Orphanet:63] [Orphanet:791] [Orphanet:886] [Orphanet:98664] [PATO:0000461] [UBERON:0001968] [UBERON:0002046] [UBERON:0010393]

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0000001 0000004 0000005 0000006 0000007 0000012 0000014 0000015 0000018 0000019 0000020 0000021 0000024 0000025 0000026 0000027 0000028 0000029 0000042 0000044 0000045 0000046

Clear

REL-2017-07-2024

HipSci - Alport Syndrome - Expression Array - July 2017
Dataset EGAD00010001376
REL-2017-07-2026

HipSci - Hypertrophic Cardiomyopathy - Expression Array - July 2017
Dataset EGAD00010001380
REL-2017-07_867

HipSci - Healthy Normals - Expression Array - July 2017
Dataset EGAD00010001330
REL-2017-07-1277

HipSci - Monogenic Diabetes - Expression Array - July 2017
Dataset EGAD00010001342
REL-2017-07-2025

HipSci - Congenital Hyperinsulinia - Expression Array - July 2017
Dataset EGAD00010001378
REL-2017-07-2029

HipSci - Macular Dystrophy - Expression Array - July 2017
Dataset EGAD00010001386
REL-2017-07-2031

HipSci - Battens Disease - Expression Array - July 2017
Dataset EGAD00010001390
REL-2017-07-2020

HipSci - Hereditary Cerebellar Ataxias - Expression Array - July 2017
Dataset EGAD00010001368
REL-2017-07-2027

HipSci - Primary Immune Deficiency - Expression Array - July 2017
Dataset EGAD00010001382
REL-2017-07-2021

HipSci - Hereditary Spastic Paraplegia - Expression Array - July 2017
Dataset EGAD00010001370

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