6365 results for "11+1双色球多少钱一注"

in 65.81 milliseconds.

• Reference epigenome Islet-derived_MSC08 h3k36me3 ChIP-Seq data generated from KEP study

  Islet-derived_MSC08 h3k36me3 ChIP-Seq paired end data

  Dataset EGAD00001007904

• Strelka somatic snv vcfs for EGAS00001004572

  Bulk Strelka somatic snv vcfs from tumour-normal analysis in EGAS00001004572

  Dataset EGAD00001006907

• GRIDSS somatic sv vcfs for EGAS00001004572

  Bulk GRIDSS somatic sv vcfs from tumour-normal analysis in EGAS00001004572

  Dataset EGAD00001006906

• STAG1 and STAG2-ChIP-seq in RAD21-mutant adult acute myeloid leukemia

  STAG1 and STAG2-ChIP-seq in RAD21-mutant adult acute myeloid leukemia

  Dataset EGAD00001015361

• Targeted capture ctDNA Library CRCQV34Run002-10

  Targeted capture ctDNA Library CRCQV34Run002-10 from patient PBC0002108, plasma baseline sample

  Dataset EGAD00001010327

• Targeted capture ctDNA Library CRCQV34Run002-12

  Targeted capture ctDNA Library CRCQV34Run002-12 from patient PBC0002459, plasma baseline sample

  Dataset EGAD00001010329

• Targeted capture ctDNA Library CRCQV34Run002-13

  Targeted capture ctDNA Library CRCQV34Run002-13 from patient PBC0002595, plasma baseline sample

  Dataset EGAD00001010330

• Targeted capture ctDNA Library CRCQV34Run002-6

  Targeted capture ctDNA Library CRCQV34Run002-6 from patient PBC0001627, plasma baseline sample

  Dataset EGAD00001010339

• Targeted capture ctDNA Library CRCQV34Run007-22

  Targeted capture ctDNA Library CRCQV34Run007-22 from patient PBC0002816, buffy coat sample

  Dataset EGAD00001010359

• Targeted capture ctDNA Library CRCQV42Run021-13

  Targeted capture ctDNA Library CRCQV42Run021-13 from patient PBC0001299, plasma baseline sample

  Dataset EGAD00001010436

• Targeted capture ctDNA Library CRCQV42Run026-4

  Targeted capture ctDNA Library CRCQV42Run026-4 from patient PBC0002872, plasma baseline sample

  Dataset EGAD00001010496

• Targeted capture ctDNA Library CRCQV42Run029-23

  Targeted capture ctDNA Library CRCQV42Run029-23 from patient PBC0004350, plasma baseline sample

  Dataset EGAD00001010516

• Targeted capture ctDNA Library CRCQV42Run033-13

  Targeted capture ctDNA Library CRCQV42Run033-13 from patient PBC0002429, buffy coat sample

  Dataset EGAD00001010552

• Targeted capture ctDNA Library CRCQV42Run033-14

  Targeted capture ctDNA Library CRCQV42Run033-14 from patient PBC0002459, buffy coat sample

  Dataset EGAD00001010553

• Targeted capture ctDNA Library CRCQV42Run034-14

  Targeted capture ctDNA Library CRCQV42Run034-14 from patient PBC0004414, buffy coat sample

  Dataset EGAD00001010568

• Targeted capture ctDNA Library CRCQV42Run039-6

  Targeted capture ctDNA Library CRCQV42Run039-6 from patient PBC0002853, plasma baseline sample

  Dataset EGAD00001010622

• Targeted capture ctDNA Library CRCQV42Run039-8

  Targeted capture ctDNA Library CRCQV42Run039-8 from patient PBC0003334, plasma baseline sample

  Dataset EGAD00001010624

• Targeted capture ctDNA Library CRCQV42Run047-6

  Targeted capture ctDNA Library CRCQV42Run047-6 from patient PBC0001255, buffy coat sample

  Dataset EGAD00001010738

• Targeted capture ctDNA Library CRCQV42Run048-24

  Targeted capture ctDNA Library CRCQV42Run048-24 from patient PBC0005531, buffy coat sample

  Dataset EGAD00001010756

• Targeted capture ctDNA Library CRCQV42Run049-22

  Targeted capture ctDNA Library CRCQV42Run049-22 from patient PBC0002481, buffy coat sample

  Dataset EGAD00001010775

• Targeted capture ctDNA Library CRCQV42Run049-23

  Targeted capture ctDNA Library CRCQV42Run049-23 from patient PBC0001409, buffy coat sample

  Dataset EGAD00001010776

• Targeted capture ctDNA Library CRCQV42Run049-4

  Targeted capture ctDNA Library CRCQV42Run049-4 from patient PBC0004537, buffy coat sample

  Dataset EGAD00001010777

• Targeted capture ctDNA Library CRCQV42Run050-19

  Targeted capture ctDNA Library CRCQV42Run050-19 from patient PBC0001527, buffy coat sample

  Dataset EGAD00001010792

• Targeted capture ctDNA Library CRCQV42Run051-19

  Targeted capture ctDNA Library CRCQV42Run051-19 from patient PBC0002294, buffy coat sample

  Dataset EGAD00001010812

• SNF_RNAseq_CD138n_20f

  TPM matrices of counts from RNA sequencing (RNAseq) from baseline CD138(–) BM fractions.

  Dataset EGAD00001011142

• RNAseq and ATACseq on HGSC lines, pre- and post-treatment with an epigenetic drug

  This study looked to determine changes in gene expression and chromatin accessibility of five HGSC cell lines, following treatment with a novel epigenetic drug. The epigenetic drug, HKMTi-1-005, is a compound with dual activity against H3K27 and H3K9 methylation. The cell lines used were PEO1, PEO4, PEA2, OVCAR5, OVCAR8.

  Study EGAS50000000047

• Bulk RNA-seq of monocytes and in vitro cultured monocyte-derived macrophages of ANCA-associated vasculitis patients with active and stable disease and healthy controls

  To study monocyte and macrophage activation in ANCA-associtated vasculitis (AAV), we performed bulk RNA sequencing of bead-selected monocytes and in vitro cultured monocyte-derived macrophages from AAV patients and healthy controls. Overview patients included for sequencing monocytes: - AAV active disease, n=4, MPO-AAV=4 - AAV remission, n=10, PR3-AAV=5, MPO-AAV=5 - Healthy controls, n=6 Overview patients included for sequencing monocyte-derived macrophages: - AAV active, n=1, PR3-AAV=1 - AAV remission, n=3, PR3-AAV=3 - Healthy controls, n=3

  Dataset EGAD50000000450

• ChIP-seq analysis of clear cell renal cell carcinoma

  In order to understand the epigenetic basis on ccRCC, we performed ChIP-seq on 3 ccRCC cell lines (786-O, A498, UMRC-2), and 1 normal kidney epithelium cell line (HK-2), cultured under normoxic (20% O2) and hypoxic (0.05% O2) conditions. This study analysed data from H3k4me1, H3K4me3, H3K27ac, H3k27me3, H3k36me3, CTCF, and HIF1A

  Study EGAS50000001322

• Common origin and somatic mutation patterns of composite lymphomas and leukemias

  The dataset contains six composite lymphomas and leukemias cases (four composite B-cell lymphomas (case 1-4), and two combinations of B-cell and T-cell lymphoma (case 5+6)). Two tumor and one non-tumor (NTC) sample were sequenced from each case after library prep with NEBNext Ultra DNA Library Prep Kit, Exome capturing was done with NimbleGen SeqCap EZ Choice kit, and sequenced on a Illumina HiSeq 2000 HO and given as fastq files. WGA (Qiagen REPLI-g kit) was used for case 2 and 3. Case 1-4 were microdisected, case 5+6 were flow-sorted.

  Dataset EGAD50000001486

• Multi-region RNA-Seq data of 10 neuroblastoma cases

  To investigate intratumour heterogeneity and to better understand tumour evolution in neuroblastoma, we have performed a multi-region RNA sequencing on a total of 51 spatially separated tumor samples from 9 primary neuroblastomas (2 low-risk, 1 intermediate-risk and 6 high-risk) and 1 relapsed neuroblastoma. We also assessed the impact of chemotherapy on the clonal expansion by sequencing tumour regions from one medium risk and one high-risk tumour for which we had matched samples obtained at diagnosis and after chemotherapy.

  Dataset EGAD00001008133

• NABUCCO cohort 1 (NCT03387761) - Neo-Adjuvant Bladder Urothelial Carcinoma COmbination-immunotherapy

  NABUCCO cohort 1 sequencing data. The dataset includes: * Whole exome DNAseq pre-treatment on tumor samples (n=24) matched with blood samples (n=24) * RNAseq pre-treatment on tumor samples (n=18) * RNAseq post-treatment on tumor samples (n=18). Not all pre-treatment samples are linked with pre-treatment samples * High coverage Whole exome DNAseq on pre-treatment tumor samples (n=3) matched with post-treatment metastasized lymph nodes isolated with laser microdissection (n=3) * All samples are labelled with the response phenotype (Complete Responder or Non-Complete Responder)

  Dataset EGAD00001006250

• Copy-choice recombination during mitochondrial L-strand synthesis causes DNA deletions

  The dataset comprises of seven samples described below 1. Muscle samples from three patients with late-onset PEO caused by compound heterozygous POLG variants M0305 POLG W748S/R1096C M1105 POLG A467T/T251I+P587L M1804 POLG A467T/X1240G+35aa 2. Muscle sample from a patient with adPEO with heterozygous TWNK variants M0230 TWNK p.Arg357Pro 3. Blood control samples from two patients with late-onset PEO caused by compound heterozygous POLG variants DNA2012-1630_S1 POLG W748S/R1096C DNA2018-0168_S2 POLG A467T/T251I+P587L 4. Muscle samples from healthy control individuals DNA2018-0172_S4 Healthy control 2 DNA2018-0173_S5 Healthy control 1

  Dataset EGAD00001004271

• Splenic Marginal Zone Lymphoma with villous lymphocytes exome sequencing

  Splenic Marginal Zone Lymphoma with villous lymphocytes exome sequencing

  Dataset EGAD00001000081

• APP-G-1

  Array data from 4778 individuals from general population of rural Uganda

  Dataset EGAD00010000965

• Transcriptome of human CD4+ T-lymphyocyte (memory-T-cells - untreated) from donor D1, replicate 2, glucose concentration 5mM

  Dataset EGAD00001008038

• Transcriptome of human CD4+ T-lymphyocyte (memory-T-cells - untreated) from donor D2, replicate 2, glucose concentration 5mM

  Dataset EGAD00001008048

• Average_5hmC_DIFF_Roadmap

  Average hydroxymethylation difference 12 months vs 0 months at Roadmap Epigenomics chromatin state annotations from different cell types. Data from 8 individuals.

  Dataset EGAD00010002415

• Sequencing data for oesophageal and related samples - OACs release 1 (RNA)

  Dataset EGAD00001002259

• Transcriptome of human CD4+ T-lymphyocyte (memory-T-cells - untreated) from donor D3, replicate 2, glucose concentration 5mM

  Dataset EGAD00001008058

• WXS_TALL_t_14_16_translocation

  Whole exome-sequencing for patients with t(14;16) translocated T-ALL.

  Dataset EGAD50000001783

• Targeted capture ctDNA Library CRCQV42Run017-8

  Targeted capture ctDNA Library CRCQV42Run017-8 from patient PBC0001224, plasma 15 month sample

  Dataset EGAD00001010415

• Targeted capture ctDNA Library CRCQV42Run039-21

  Targeted capture ctDNA Library CRCQV42Run039-21 from patient PBC0003014, plasma 3 month sample

  Dataset EGAD00001010616

• Targeted capture ctDNA Library CRCQV42Run024-9

  Targeted capture ctDNA Library CRCQV42Run024-9 from patient PBC0003641, plasma baseline sample

  Dataset EGAD00001010475

• Targeted capture ctDNA Library CRCQV42Run032-8

  Targeted capture ctDNA Library CRCQV42Run032-8 from patient PBC0001589, buffy coat sample

  Dataset EGAD00001010547

• Targeted capture ctDNA Library CRCQV42Run044-18

  Targeted capture ctDNA Library CRCQV42Run044-18 from patient PBC0003376, plasma 12 month sample

  Dataset EGAD00001010668

• Targeted capture ctDNA Library CRCQV42Run046-20

  Targeted capture ctDNA Library CRCQV42Run046-20 from patient PBC0001176, plasma 3 month sample

  Dataset EGAD00001010711

• Targeted capture ctDNA Library CRCQV42Run035-24

  Targeted capture ctDNA Library CRCQV42Run035-24 from patient PBC0004565, plasma 9 month sample

  Dataset EGAD00001010588

• Targeted capture ctDNA Library CRCQV42Run045-12

  Targeted capture ctDNA Library CRCQV42Run045-12 from patient PBC0001068, plasma 3 month sample

  Dataset EGAD00001010683

• Targeted capture ctDNA Library CRCQV42Run041-24

  Targeted capture ctDNA Library CRCQV42Run041-24 from patient PBC0005116, plasma 3 month sample

  Dataset EGAD00001010633

• Reference epigenome SMC07 mRNA-Seq data generated from KEP study

  SMC07 mRNA-Seq paired end data

  Dataset EGAD00001007174