17850 results for "the best way to get coins in fc 26 Navštivte Buyfc26coins.com Společnost známá transparentními transakcemi..CQ2q"

in 111.78 milliseconds.

• TOPARP-B patient cell-free DNA WGS

  Sequencing files for TOPARP-B patients as described in manuscript

  Study EGAS50000000280

• Clonal IGHV rearrangements in IGH+ and IGHUND HGBCL-DH-BCL2(-BCL6)

  PCR-based VDJ profiling in IGH+ and IGHUND HGBCL-DH-BCL2(-BCL6) lymphomas

  Dataset EGAD50000001523

• Targeted_NanoSeq___Thyroid

  Targeted NanoSeq in thyroid from a number of donors, both healthy and with pathology.

  Study EGAS00001007647

• McGill EMC Release 4 in tissue "skeletal muscle tissue"

  McGill EMC Release 4 in tissue "skeletal muscle tissue"

  Dataset EGAD00001001288

• Mediator ChIP-Seq datasets in human islets

  6 ChIP-Seq datasets of Mediator in human pancreatic islets from 6 donors

  Dataset EGAD00001005202

• Cohesin ChIP-Seq datasets in human islets

  3 ChIP-Seq datasets of Cohesin in human pancreatic islets from 3 donors

  Dataset EGAD00001005203

• Cardiac fibroblast DAC

  DAC for reviewing requests to access data on cardiac fibroblasts as described by Aguado-Alvaro et al (Nature Communications, 2025)

  Dac EGAC50000000479

• Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases

  Study EGAS00001007783

• "Single nucleotide variant detection in multiple foci of three prostate cancer tumors"

  "Single nucleotide variant detection in multiple foci of three prostate cancer tumors"

  Dataset EGAD00001000035

• "Copy number variant detection in multiple foci of three prostate cancer tumors"

  "Copy number variant detection in multiple foci of three prostate cancer tumors"

  Dataset EGAD00001000036

• Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___POL___TGS_

  Somatic mutations (burdens and signatures) and clonal dynamics in individuals with germline DNA polymerase mutations.

  Study EGAS00001003754

• Exome_NanoSeq__Thyroid_

  Exome NanoSeq in thyroid from a number of donors, both healthy and with pathology.

  Study EGAS00001007175

• Multiomic Dissection of Movement and Neurocognitive Toxicity Following BCMA-Targeting CAR T Therapy

  We report a case of parkinsonism following treatment with ciltacabtagene autoleucel. To investigate underlying mechanisms, we performed a multi-pronged longitudinal analysis using single-cell RNA/TCR-sequencing including both cerebrospinal fluid (CSF) and peripheral blood samples, spanning a time frame over 6 month after CAR T cell therapy.

  Study EGAS50000001634

• 10X snRNA-seq data from human FCDII postoperative brain tissues with mTOR pathway mutations

  Focal cortical dysplasia type II (FCDII) is linked to mTOR pathway mutations and drug-resistant epilepsy. Using 10X snRNA-seq on postoperative FCDII brain tissues, we characterized transcriptional alterations across cell types, revealing mTOR-related dysregulation. These findings provide insights into FCDII pathology and potential therapeutic target

  Study EGAS50000000964

• Single cell RNA sequencing of CD19 CAR T-cell infusion products

  We performed single cell RNA sequencing of remnants from CD19 CAR T-cell infusion products used for standard of care treatment for relapsed/refractory large B-cell lymphoma. Libraries were prepared using 10X 5’ GEX chemistry and sequenced on an Illumina HiSeq 4000 to obtain >50,000 reads per cell.

  Study EGAS00001004576

• Intellectual Disability cases with parents (trios) or affected sibs (sibpairs)

  Samples from ID cases negative for CNV through array-CGH were submitted to exome sequencing. Families with one affected individual underwent trio exome sequencing for identification of de novo variants. Families with more than one affected child underwent sibpair sequencing for identificatio of shared recessive or x-linked variants.

  Study EGAS00001003968

• Whole-Genome Sequencing of 128 Ashkenazi Jewish individuals

  We sequenced 128 individuals of Ashkenazi Jewish ancestry. All individuals were controls in other studies: (1) Longevity (Gil Atzmon's lab; Albert Einstein College of Medicine), n=74. (2) Parkinson's disease (Lorraine Clark's lab; Columbia University Medical Center), n=54. Whole-genome, high-coverage (50x) sequencing was performed by Complete Genomics in 2012 and 2013.

  Study EGAS00001000664

• Transcriptome sequencing of myelodysplasia

  Transcriptome sequencing was performed on 214 patients with myelodysplasia in this study. RNA was obtained from bone marrow CD34+ cells (n=100) and/or bone marrow mononuclear cells (n=165). Transcriptome sequencing was performed for both cell fractions in 51 patients. We also studied bone marrow CD34+ cells and bone marrow mononuclear cells obtained from three healthy adults each.

  Study EGAS00001002346

• Evolutionary analysis of pancreatic neoplastic cysts through whole-exome and targeted sequencing

  Intraductal papillary mucinous neoplasms (IPMNs) and mucinous cystic neoplasms (MCNs) are non-invasive neoplasms that are often observed in association with invasive pancreatic cancers, but their origins and evolutionary relationships are poorly understood. In this study, we analyzed 148 samples from IPMNs, MCNs, and small associated invasive carcinomas from 18 patients using whole exome or targeted sequencing.

  Study EGAS00001004473

• ChIP-seq bulk

  This dataset gather ChIP-seq data produced by immunoprecipitating CTCF factor in own laboratory in MM.1S cell line in EtOH and Dex conditions. It also gather ChIP-seq dataset produced by external laboratory (Active Motif) for H3K27ac mark and GR transcription factor in same cell line and conditions ( MM.1S ETOH/Dex)

  Dataset EGAD00001011136

• DAC for "Capturing disease severity in LIS1-lissencephaly reveals proteostasis dysregulation in patient-derived forebrain organoids" with Julia Ladewig(Julia.ladewig@zi-mannheim.de), Moritz Mall(m.mall@dkfz-heidelberg.de), and Matteo Gasparotto(matteo.gasparotto@zi-mannheim.de)

  Dac EGAC00001003588

• Chromatin accessibility in OCI-AML22 cells

  ATAC-seq performed in OCI-AML22 subpopulations sorted based on CD34 and CD38 status

  Dataset EGAD50000001631

• Liquid Biopsy by NGS show differences in CRC stage

  Exome sequencing from cfDNA blood samples. 30 sets of 2x76 Illumina reads in Fastq format.

  Dataset EGAD00001004307

• McGill EMC Release 4 in tissue "Brodmann (1909) area 11"

  McGill EMC Release 4 in tissue "Brodmann (1909) area 11"

  Dataset EGAD00001001284

• McGill EMC Release 4 in tissue "Brodmann (1909) area 44"

  McGill EMC Release 4 in tissue "Brodmann (1909) area 44"

  Dataset EGAD00001001285

• Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma

  Caracterization of somatic variants in patients with OpSCC

  Dataset EGAD00001006151

• Inherited Corneal Dystrophies - Institute of Ophthalmology, University College London (IoO, UCL)

  DAC created for access to data published by Dr. Alice E Davidson

  Dac EGAC50000000213

• High throughput profiling of undifferentiated pleomorphic sarcomas identifies two main subgroups with distinct immune contexture, clinical outcome and sensitivity to targeted therapies

  Study EGAS00001004612

• Dataset for study EGAS00001004946 (Endothelium-derived stromal cells contribute to bone marrow niche formation)

  Dataset EGAD00001006914

• Non-Hodgkin Lymphoma WES Data Access Committee

  DAC for controlled access to whole exome sequencing (WES) data from NHL patients at University of Tabuk

  Dac EGAC50000000998

• Characterization of HCV-specific CD4 T cells during DAA-Therapy

  To be added...

  Dataset EGAD00001005432

• Morphological and gene expression changes in SCA1 cerebral organoids suggest neurodevelopmental disease characteristics

  Cerebral organoids were generated from controls, individuals with SCA1 and gene-edited SCA1 hiPS cells. At day 31 and day 60, RNA sequencing was performed showing differential of several genes involved in neural development.

  Study EGAS50000001720

• RESOLVE_trial_targeted_sequencing_data

  RESOLVE: Abemaciclib + Letrozole +/_- Metformin, Zotatifin, or Gedatolisib in Endometrial or Low-Grade Serous Ovarian Cancer

  Study EGAS50000001202

• Deep RNA sequencing in CLL

  Deep RNA sequencing in CLL

  Dataset EGAD00001000258

• Epilepsy_related_sudden_death

  These samples include exome sequences of samples from patients who suffered Sudden Unexplained Death in Epilepsy

  Study EGAS00001000352

• Mutational_signatures_and_clonal_dynamics_in_normal_human_tissues

  Somatic mutations (burdens and signatures) and clonal dynamics in normal human tissues

  Study EGAS00001002471

• GoNL raw sequence data in fastq format

  Raw sequencing data for all samples in fastq format.

  Dataset EGAD00001000821

• JAK and STAT alterations in CD30 positive LPD

  JAK and STAT alterations in CD30 positive LPD, panel sequencing, 12 cutaneous lymphoma patients, 40 samples

  Dataset EGAD00001005801

• MDS_Sequential_Treatment_Validation

  Validations of variants identified by exome sequencing in sequential samples derived after treatment cycle with AZA.

  Study EGAS00001000703

• Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___POL___WGS

  Somatic mutations (burdens and signatures) and clonal dynamics in individuals with germline DNA polymerase mutations.

  Study EGAS00001003682

• Exome_NanoSeq__Buccals_

  Exome NanoSeq in buccal swab samples obtained from patients with a wide range of clinical phenotypes.

  Study EGAS00001007316

• TLR7 variants in human lupus patients

  Set of 2 bam files from patients affected with Lupus. Fastq alignments for exonic variants present in TLR7 gene.

  Dataset EGAD00001008534

• Study of biomarkers implicated in radio-immunotherapy response in metastatic cancer

  RNA sequencing data of tumors from 53 patients with advanced or metastatic cancer

  Dataset EGAD50000001644

• RNA-seq in insulinomas

  RNA-seq datasets in human insulinoma samples

  Dataset EGAD50000000462

• Somatic mutation of SF3B1 in myelodysplasia with ring sideroblasts and other cancers

  Somatic mutation of SF3B1 in myelodysplasia with ring sideroblasts and other cancers

  Dataset EGAD00001000045

• WTCCC2 project Glaucoma (GL) samples

  A WTCCC2 genome-wide association study for glaucoma (GL) in Australian individuals of European descent.

  Study EGAS00001000624

• Cell_lines_with_telomere_fusion_induced_rearrangements

  Whole-genome somatic rearrangement and point mutation analysis in cell lines with induced telomere fusions.

  Study EGAS00001001059

• McGill EMC Release 4 in tissue "venous blood" for cell type "eosinophil"

  McGill EMC Release 4 in tissue "venous blood" for cell type "eosinophil"

  Dataset EGAD00001001281

• McGill EMC Release 4 in tissue "venous blood" for cell type "Monocyte"

  McGill EMC Release 4 in tissue "venous blood" for cell type "Monocyte"

  Dataset EGAD00001001282

• Amplicon sequencing

  Fastq files from amplicon sequencing in 106 Multiple Sclerosis patients and 105 healthy volunteers in CD4 T cells, CD8 T cells and genomic DNA using PE300 Illumina MiSeq.

  Dataset EGAD00001005774