1021 results for "中国疾控中心2024年12月传染病死亡病例统计数据"

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• 12 Pediatric B-cell precursor acute lymphoblastic leukemia samples with very early relapse

  Sequencing data (BAM/CRAM) of diagnosis-relapse pairs of 12 children who relapsed very early, followed by a deep-sequencing validation of all identified mutations.

  Dataset EGAD00001008309

• Targeted sequencing data and shallow whole genome sequencing data of Follicular lymphoma.

  Contain data of 2 studies 1: 82 nodal stage 1 FL cases and 139 stage III/IV cases 2: 44 watch and wait stage III/IV and 46 Immediate treatment stage III/IV targeted sequencing data of 369 genes and 12 translocation regions whole genome shallow sequencing data

  Study EGAS00001005755

• Pediatric B-cell precursor acute lymphoblastic leukemia samples with very early relapse

  In this study we performed a genomic analysis of diagnosis-relapse pairs of 12 children who relapsed very early, followed by a deep-sequencing validation of all identified mutations. In addition, we included one case with a good initial treatment response and on-treatment relapse at the end of upfront therapy.

  Study EGAS00001005615

• Oxford Nanopore RNA sequencing for HLA typing

  A targeted RNA-based method for typing of 12 classical HLA genes using Oxford Nanopore sequencing. In the method, were enriched HLA genes from cDNA of 50 individuals using gene-specific reverse primers. The library molecules were then barcoded, pooled into 2 separate gene pools, and sequenced on MinION R9.4 SpotON flow cells.

  Study EGAS00001004918

• Personalised Mapping of Tumour Development in Synchronous Colorectal Cancer Patients

  We performed an in-depth characterisation of 12 tumours from 3 syCRC patients by analysing histopathological, whole genome sequencing and RNA-sequencing data. We assessed the extent of genetic overlap between synchronous tumours and examined associations between clinicopathological information and the molecular, microbial and immune features of each tumour genome.

  Study EGAS00001004413

• Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkers

  This project includes RNA-sequencing data from human FSHD and control skeletal muscle biopsies. This project includes data from 28 FSHD patients (total 37 samples, including vastus lateralis and tibialis anterior muscles) and 12 control individuals (total 24 samples, including vastus lateralis and tibialis anterior muscles).

  Study EGAS00001005782

• PhIP-seq of Japanese patients with SLE

  Bacteriophage Immunoprecipitation Sequencing (PhIP-Seq) datasets of three eHHV-6B-positive SLE patients (three technical replicates), six eHHV-6B-negative SLE patients (three technical replicates), and a negative control lacking sera or plasma (12 technical replicates; Illumina NextSeq) and sequencing data of HHV-6 peptide phage library (two technical replicates; Illumina NextSeq).

  Study EGAS00001007955

• Colorectal cancer cells possess an equipotent capacity to enter a developmental pausing-like state to survive chemotherapy

  Dataset EGAD00001006847

• Exome sequencing of patients with structural brain malformations

  Exome sequencing of 12 DNA samples obtained from patients with structural brain malformations.

  Dataset EGAD00001000345

• Single-Cell Multi-Omic Analysis of the Vestibular Schwannoma Ecosystem Uncovers a Nerve Injury-Like State

  Vestibular schwannomas are benign tumors that can lead to significant morbidity, including hearing loss, facial nerve paralysis and obstructive hydrocephalus. The genomic landscape of vestibular schwannomas is relatively bland and the molecular pathophysiology of vestibular schwannomas is poorly understood. Therefore, we performed single cell RNA sequencing on 15 sporadic vestibular schwannomas, with paired single cell ATAC sequencing (n = 6) and whole exome sequencing (n = 12) to perform a detailed characterization of the vestibular schwannoma tumor microenvironment at the transcriptional and epigenetic level. We validated our results by analyzing bulk RNA sequencing data from 22 newly sequenced vestibular schwannomas and 173 previously sequenced bulk RNA sequencing data from 195 vestibular schwannomas. Data available in dbGaP include whole exome sequencing of 12 tumors and matched blood samples. Matching single cell RNA sequencing and single cell ATAC sequencing data is available via NCBI GEO.

  Study phs003318

• SPECTA RP-1759-AYA Sarcoma cohort

  EORTC-SPECTA RP1759 study focuses on cancers in adolescent and young adult (AYA), age 12 to 29 years. This study explicitly recruited AYA patients and therefore collected empirical data to bridge the molecular gap between pediatric and adult oncology. The initial pilot study, activated in February 2019 across Europe, aimed to recruit 100 AYA patients (aged 12-29 years) with newly diagnosed or relapsed high-grade gliomas and high-grade bone and soft tissue sarcomas. The primary objective of the pilot is to determine feasibility and recruitment rates. Here we submit the data from patients with newly diagnosed, recurrent intermediate or high-grade sarcoma that were collected and analyzed during the study. More specifically, we submit raw FASTQ files obtained from whole exome sequencing (WES) of matching tumor and blood samples, tumor RNA sequencing and DNA methylation profiling.

  Study EGAS00001005840

• ICGC prostate cancer RNA sequencing

  ICGC prostate cancer RNA sequencing

  Dataset EGAD00001000305

• ICGC prostate cancer MBD sequencing (DNA methylation)

  Dataset EGAD00001000632

• Sample metadata

  Sample metadata for this experiment. Includes treatment and donor derivation information.

  Dataset EGAD50000000827

• TCR β-chain repertoire characterization of regulatory and conventional T cells in breast tumors from breast cancer patients.

  Dataset EGAD00001006428

• DIPG_ICR_WES

  Whole exome sequencing of 6 tumour and normal pairs of diffuse intrinsic pontine glioma (DIPG)

  Dataset EGAD00001000706

• SNParray_Human_blastocyst_samples

  Single blastomeres from blastocyst and familial samples for haplotyping and copy-number profiling via SNP array

  Dataset EGAD00010002220

• Linked-reads for Juvenile Pilocytic Astrocytomas

  Matched tumor-normal data for 6 JPAs. Generated using 10X Genomics Linked-reads

  Dataset EGAD00001011114

• GEP_DKFZ_JMML_DBL

  Gene expression analysis from primary human JMML samples using Illumina Human HT-12 v4

  Dataset EGAD00010001430

• SNParray_PGT_samples_scGBS

  PGT samples for haplotyping and copy-number profiling via SNP array

  Dataset EGAD00010002169

• SNParray_HapMap_samples_scGBS

  HapMap samples for haplotyping and copy-number profiling via SNP array

  Dataset EGAD00010002168

• scRNAseq data of HGSOC patients before and after treatment

  scRNAseq data of HGSOC patients before and after treatment

  Dataset EGAD50000000191

• H3K27ac ChIP-seq in Insulinomas

  H3K27ac ChIP-seq datasets in human insulinoma samples

  Dataset EGAD50000000461

• Low input LC (ISC)

  R&D project to develop low input library construction methods.

  Dataset EGAD00001003254

• AML exome sequencing

  Raw data (fastq files) from whole exome sequencing of AML patients (paired diagnosis and complete remission samples)

  Dataset EGAD00001002116

• Single-nuclei multiomic analysis of KOLF2.1J human induced pluripotent stem cells-derived differentiated dopaminergic neurons

  Datasets consists of 12 samples of nuclei from hIPSCs differentiated optimized protocols for generating dopaminergic neurons. 6 single nuclei (RNA-ATAC) samples of XMAS protocol with cells collected at days 0,11,16,28,42 and 56 after differentiation. 3 snRNA-seq samples from AMS protocol of cells collected at days 14,16 and 28 after differentiation and 3 snRNA-seq samples with AMS protocol until day 14 grafted and grafts processed after 5 months grafting.

  Dataset EGAD50000002054

• Columbia Alzheimer's sample (white matter)

  The Columbia Alzheimer’s dataset (white matter) consists of 24 white matter individuals (12 controls, 12 cases). A total of 12,000 estimated cells from each sample were loaded on the 10x Single Cell Next GEM G Chip. cDNA libraries were prepared using the Chromium Single Cell 3’ Library and Gel Bead v3 kit according to the manufacturer’s instructions. cDNA libraries were sequenced using the Illumina NovaSeq 6000 System and NovaSeq 6000 S2 Reagent Kit v1.5 (100 cycles), aiming at a sequencing depth of minimum 30K reads/nucleus.

  Dataset EGAD00001009168

• Methylation files for Roussel-ATRT-TM

  Methylation files for Roussel-ATRT-TM paper titled "Atypical teratoid/ rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities"

  Dataset EGAD00010002357

• Whole exome sequencing of matched tumor-normal brain metastases

  Whole exome sequencing of matched tumor (brain metastasis) -normal (blood) from 6 patients.

  Dataset EGAD00001006453

• Evaluation of PCR library method on whole genome samples

  Evaluation of PCR library method on whole genome samples

  Dataset EGAD00001000252

• Human Epidermis scRNA

  Single cell RNA-seq analysis of human skin.

  Dataset EGAD00010001620

• 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

• Hipo-032 Metastasome of Colorectal Cancer

  Whole genome sequencing of Control (blood), Tumor and metastasis triplets for 12 samples.

  Dataset EGAD00001003965

• Targeted capture ctDNA Library CRCQV42Run017-13

  Targeted capture ctDNA Library CRCQV42Run017-13 from patient PBC0002383, plasma 12 month sample

  Dataset EGAD00001010406

• Targeted capture ctDNA Library CRCQV42Run017-18

  Targeted capture ctDNA Library CRCQV42Run017-18 from patient PBC0002294, plasma 12 month sample

  Dataset EGAD00001010410

• Targeted capture ctDNA Library CRCQV42Run035-10

  Targeted capture ctDNA Library CRCQV42Run035-10 from patient PBC0002872, plasma 12 month sample

  Dataset EGAD00001010577

• Targeted capture ctDNA Library CRCQV42Run043-7

  Targeted capture ctDNA Library CRCQV42Run043-7 from patient PBC0001589, plasma 12 month sample

  Dataset EGAD00001010657

• Targeted capture ctDNA Library CRCQV34Run015-9

  Targeted capture ctDNA Library CRCQV34Run015-9 from patient PBC0001627, plasma 12 month sample

  Dataset EGAD00001010386

• Targeted capture ctDNA Library CRCQV42Run017-10

  Targeted capture ctDNA Library CRCQV42Run017-10 from patient PBC0002255, plasma 12 month sample

  Dataset EGAD00001010403

• Targeted capture ctDNA Library CRCQV42Run035-13

  Targeted capture ctDNA Library CRCQV42Run035-13 from patient PBC0001859, plasma 12 month sample

  Dataset EGAD00001010580

• Targeted capture ctDNA Library CRCQV42Run036-21

  Targeted capture ctDNA Library CRCQV42Run036-21 from patient PBC0004173, plasma 12 month sample

  Dataset EGAD00001010600

• Targeted capture ctDNA Library CRCQV42Run036-8

  Targeted capture ctDNA Library CRCQV42Run036-8 from patient PBC0003641, plasma 12 month sample

  Dataset EGAD00001010605

• Targeted capture ctDNA Library CRCQV42Run044-16

  Targeted capture ctDNA Library CRCQV42Run044-16 from patient PBC0005586, plasma 12 month sample

  Dataset EGAD00001010666

• 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 CRCQV42Run045-8

  Targeted capture ctDNA Library CRCQV42Run045-8 from patient PBC0006360, plasma 12 month sample

  Dataset EGAD00001010700

• Targeted capture ctDNA Library CRCQV42Run046-10

  Targeted capture ctDNA Library CRCQV42Run046-10 from patient PBC0001552, plasma 12 month sample

  Dataset EGAD00001010701

• HGP-clean

  Himalayan population genetic study QC filtered data

  Dataset EGAD00010001471

• RNAseq counts

  RNA-seq data from ILC samples. This dataset includes raw, unnormalized counts per gene, per sample.

  Dataset EGAD50000000826

• AFB1 Mutation Signature Dataset

  This dataset contains whole exome sequence of six HCC patients from Qidong China who are very likely exposed to aflatoxin.

  Dataset EGAD00001003194

• Prostate WGS data (late onset)

  Whole genome sequencing for 12 late onset prostate cancer tumor/control pairs (ICGC)

  Dataset EGAD00001003290