21167 results for "Buy fc 26 coins Buyfc26coins.com is EA Sports official for FC 26 coins The process was smooth and quick..ivNx"

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• MMR (DNA mismatch repair) pathway in human samples

  This data are related to the manuscript by Germano et al. Ms2016-04-06029

  Study EGAS00001002694

• Germline sequencing

  Detection of SNVs/indels in the germline of pediatric cancer patients with a focus on CHEK2 germline variants.

  Study EGAS00001006254

• Germline sequencing

  Detection of SNVs/ indels in the germline of pediatric cancer patients with a focus on CHEK2 germline variants

  Study EGAS00001006705

• HCA_Immune_Adult_CIDP_RNA_Managed_Access

  Leveraging single-cell sequencing technologies to shed light on the immune aetiology of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)

  Study EGAS00001007419

• 30X WGS sequencing of 100 individuals from the general Greek population

  This project entailed generation of high depth WGS (30x) of 100 individuals from the general Greek population.

  Dataset EGAD00001001440

• bam files Targeted BS

  Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015

  Dataset EGAD00001001667

• BAM Files MBD-SEQ

  Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015

  Dataset EGAD00001001668

• Characterising the evolutionary dynamics of cancer proliferation in single-cell clones with SPRINTER

  Characterising the evolutionary dynamics of cancer proliferation in single-cell clones with SPRINTER

  Dataset EGAD00001015411

• Transcriptional profiling and clonality analysis of peripheral blood B cells and small intestinal plasma cells in celiac disease

  Single-cell RNA-seq and BCR sequencing and/or inference of sorted IgA+ peripheral blood B-lineage cells and small intestinal plasma cells of untreated celiac disease patients.

  Study EGAS50000000229

• Solve-RD_EuroNMD_cohort-1_DF1+2_V1

  Solve-RD data submitted to the ERN-EuroNMD cohort for re-analysis (Data freeze 1+2) v1

  Dataset EGAD00001009768

• Genetic and epigenetic analysis of individuals with porokeratosis

  We performed genome sequencing���including whole-exome sequencing (WES), whole-genome sequencing (WGS), long-read WGS, and amplicon-seq���along with SNP array, methylation array, and RNA-seq on samples of epidermis (both lesion and non-lesion), peripheral blood, and/or cultured keratinocytes from individuals with porokeratosis.

  Study JGAS000684

• Variant calling for UPST-SCCHN3 cohort

  Tumor versus Germline variant calling on UPST-SCCHN3 cohort

  Dataset EGAD50000002178

• NANOPORE_TALL_t_14_16_translocation

  Nanopore sequencing for patients with t(14;16) translocated T-ALL

  Dataset EGAD50000001785

• WXS_TALL_t_14_16_translocation

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

  Dataset EGAD50000001783

• WGS_TALL_t_14_16_translocation

  WGS data for patients with t(14;16) translocated T-ALL.

  Dataset EGAD50000001782

• WGS data for medulloblastoma samples (MDT-AP)

  WGS data of medulloblastoma tumor/control pairs.

  Dataset EGAD00001003125

• GM18507 direct library preparation (DLP) single-cell genomes

  Microfluidic direct library preparation (DLP) single-cell whole-genome BAM files for near-diploid immortalized lymphoblastoid cell line GM18507.

  Dataset EGAD00001003148

• Sequencing data for ICGC Oesophageal Adenocarcinoma tissue samples - barretts_1

  Samples from Ross Innes et. al 2015 - doi:10.1038/ng.3357

  Dataset EGAD00001001394

• Low-depth whole genome sequencing across multiple isolated populations

  Isolated populations have unique population genetics characteristics that can help boost power in genetic association studies for complex traits. Leveraging these advantageous characteristics requires an in-depth understanding of parameters that have shaped sequence variation in isolates. This study performs a comprehensive investigation of these parameters using low-depth whole genome sequencing (WGS) across multiple isolates.

  Dataset EGAD00001002014

• single cell data from HPV-positive head and neck cancer patients receiving induction CTLA-4 and PD-1 immune checkpoint blockade

  Baseline and on-treatment tumor samples from human papillomavirus-positive oropharynx cancer patients receiving anti-CTLA-4 and anti-PD-1 immune checkpoint blockade were analyzed by single-cell RNA and TCR sequencing.

  Study EGAS50000000335

• A110632A

  Whole genome sequencing for single cells for library A110632A 1151 cells; filetype=bam

  Dataset EGAD00001007094

• A110632B

  Whole genome sequencing for single cells for library A110632B 892 cells; filetype=bam

  Dataset EGAD00001007095

• A118833A

  Whole genome sequencing for single cells for library A118833A 919 cells; filetype=bam

  Dataset EGAD00001007096

• A118833B

  Whole genome sequencing for single cells for library A118833B 1147 cells; filetype=bam

  Dataset EGAD00001007097

• A118845B

  Whole genome sequencing for single cells for library A118845B 1209 cells; filetype=bam

  Dataset EGAD00001007098