6365 results for "11+1双色球多少钱一注"

in 8.94 milliseconds.

• Genome-wide data for 11 Roma individuals

  This dataset includes genome-wide autosomal array data for 11 Iberian Roma individuals used in the Merchero project.

  Dataset EGAD00001007773

• Target sequencing of 11 hereditary breast cancer genes in Japanese

  We performed a case control association study for variants in coding regions of 11 hereditary breast cancer genes in 7,051 female unselected breast cancer patients, 11,241 female controls, 53 male patients, and 12,490 male controls of Japanese ancestry. The 11 genes were ATM, BRCA1, BRCA2, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, STK11, and TP53.

  Study JGAS000140

• Human Single-Oocyte Transcriptome - Control and Cannabis Treated

  RNAseq data of human single oocytes exposed to THC and its metabolites, (mean concentration measured in the follicular fluid, THC1, n=95, 25 ng/mL Δ9-THC, 5 ng/mL 11-OH-THC, 50 ng/mL 11-COOH-THC) or a supraphysiologic, THC2, n=93, 100 ng/mL Δ9-THC, 50 ng/mL 11-OH-THC, 200 ng/mL 11-COOH-THC).

  Dataset EGAD50000001534

• Whole genome sequencing, DNA methylation, and gene expression data from gastrointestinal stromal tumor 30 patients

  We performed WGS along with genome-wide DNA methylation and gene expression analyses in 30 GIST cases to determine the genomic and epigenomic differences between KIT exon 11 557���558 deletions and other KIT exon 11 mutations.

  Study JGAS000604

• UK10K_NEURO_FSZ REL-2012-11-27

  UK10K_NEURO_FSZ REL-2012-11-27

  Dataset EGAD00001000318

• BLUEPRINT release August 2015, Bisulfite-Seq for effector memory CD8-positive, alpha-beta T cell, on genome GRCh38

  Bisulfite-Seq data for 1 effector memory CD8-positive, alpha-beta T cell sample(s). 11 run(s), 1 experiment(s), 1 alignment(s) on human genome GRCh38. Part of BLUEPRINT release August 2015. Analysis documentation available at http://ftp.ebi.ac.uk/pub/databases/blueprint/releases/20150820/homo_sapiens/README_bisulphite_analysis_CNAG_20150820

  Dataset EGAD00001001583

• Whole genome sequencing of 76 tumor and normal samples from 11 SI-NET patients

  We have sampled 11 patients with multifocal SI-NETs. The complete genome sequences of 65 tumor and tissue samples including 42 intestinal lesions, 14 adjacent lymph node metastases, 5 distant metastases, as well as of 4 normal tissue and 11 normal blood samples were determined. This allowed elucidation of phylogenetic relationships between tumors within individual patients.

  Study EGAS00001005096

• Single-cell long-read transcriptomes from CH, MDS and AML patients with CH mutations

  Single-cell long-read (ONT) transcriptome sequencing from CH (n = 3), MDS (n = 5, MDS02 in 2 replicates) and AML (n =1, in 2 replicates) samples with mutations in splicing factors (SF3B1 - n = 8, U2AF1 n = 1) or transcription regulators (DNMT3A - CH04). Full length cDNA from 10x Genomics 3' V3.

  Dataset EGAD00001011282

• The natural history of clonal haematopoiesis: phase 6 targeted

  Deep targeted sequencing of 56 genes associated with clonal haematopoiesis and haematological malignancy in peripheral blood-derived DNA from 11 older adults, each previously sampled 2-5 times over the preceding ~13 years.

  Dataset EGAD00001007683

• Codelink_HWG_CLD_B

  Codelink Human Whole Genome from Blood taken at 72 hours after birth (11 cases)

  Dataset EGAD00010001424

• Single-cell RNA sequencing data of peripheral blood mononuclear cells obtained from 30 ATL patients, 11 HTLV-1-infected asymptomatic carriers, and 4 healthy donors.

  Single-cell RNA sequencing (scRNA-seq) data of peripheral blood mononuclear cells (PBMCs) obtained from 30 ATL patients (34 samples including 4 sequential ones), 11 HTLV-1-infected asymptomatic carriers, and 4 healthy donors.

  Dataset EGAD00001007015

• UK10K_NEURO_ASD_TAMPERE REL-2012-11-27

  UK10K_NEURO_ASD_TAMPERE REL-2012-11-27

  Dataset EGAD00001000314

• UK10K_NEURO_FSZNK REL-2012-11-27

  UK10K_NEURO_FSZNK REL-2012-11-27

  Dataset EGAD00001000332

• UK10K_NEURO_ASD_MGAS REL-2012-11-27

  UK10K_NEURO_ASD_MGAS REL-2012-11-27

  Dataset EGAD00001000312

• UK10K_NEURO_ASD_SKUSE REL-2012-11-27

  UK10K_NEURO_ASD_SKUSE REL-2012-11-27

  Dataset EGAD00001000313

• UK10K_NEURO_ASD_BIONED REL-2012-11-27

  UK10K_NEURO_ASD_BIONED REL-2012-11-27

  Dataset EGAD00001000310

• UK10K_NEURO_ASD_FI REL-2012-11-27

  UK10K_NEURO_ASD_FI REL-2012-11-27

  Dataset EGAD00001000311

• UK10K_NEURO_ASD_GALLAGHER REL-2012-11-27

  UK10K_NEURO_ASD_GALLAGHER REL-2012-11-27

  Dataset EGAD00001000316

• UK10K_NEURO_IMGSAC REL-2012-11-27

  UK10K_NEURO_IMGSAC REL-2012-11-27

  Dataset EGAD00001000320

• UK10K_NEURO_IOP_COLLIER REL-2012-11-27

  UK10K_NEURO_IOP_COLLIER REL-2012-11-27

  Dataset EGAD00001000321

• UK10K_NEURO_UKSCZ REL-2012-11-27

  UK10K_NEURO_UKSCZ REL-2012-11-27

  Dataset EGAD00001000335

• 11 plasma cases and 4 urine cases (mouse)

  11 plasma cases and 4 urine cases (mouse)

  Dataset EGAD00001009829

• RNAseq of samples from CLL patients treated with ibrutinib in vivo

  The dataset contains RNA sequencing data from 22 paired samples of 11 patients before and during ibrutinib therapy (median time on therapy 2 weeks; range 1-12 weeks). The sequencing was performed in two batches.

  Dataset EGAD50000000879

• Pheochromocytoma paraganglioma single nuclei RNA-seq

  Single nuclei RNA sequencing (snRNA-seq) on tissue samples from 11 patients (SDHB and RET). Files are fastq files of 10x-5'scRNAseq libraries.

  Dataset EGAD00001008739

• Identifying mutations in patient-derived melanoma DCC lines

  To identify mutations that cause resistance, we analyzed two patient-derived cell lines: Mel-DCC-11 (the parental line, sensitive to the BRAF inhibitor) and Mel-DCC-11-R (resistant to the BRAF inhibitor). We employed targeted-panel sequencing to examine the coding sequences of 410 cancer-associated target genes.

  Study EGAS50000001225