14666 results for "PLOS+ONE+Pennsylvania+German+ACS+language+code+pdc+open+access+study"

in 14.16 milliseconds.

• Exome analysis of cardiomyopathy patients with DSG2 variants

  This research aims to identify genetic background of cardiomyopathy patients with DSG2 pathogenic variants by exome analysis.

  Study JGAS000565

• Exome analysis of cardiomyopathy patients with TNNT2 variant

  This research aims to identify genetic background of cardiomyopathy patients with TNNT2 pathogenic variants by exome analysis.

  Study JGAS000567

• Exome analysis of cardiomyopathy patients with PKP2 variants

  This research aims to identify genetic background of cardiomyopathy patients with PKP2 pathogenic variants by exome analysis.

  Study JGAS000566

• NGS sequencing for genes from the patients of OU Genome Project

  This research aims to identify disease related HLA alleles by genome analysis for cardiac sarcoidosis.

  Study JGAS000568

• Whole genome sequencing analysis of colorectal cancers

  Whole genome sequencing analysis of colorectal cancers with MSI or MSS and their immuno-genomic features

  Study JGAS000157

• Targeted Capture DNA Sequencing

  We performed targeted capture DNA sequencing for 29 genes in extranodal NK/T-cell lymphoma, nasal type (n=67).

  Study JGAS000548

• Long read whole genome sequencing data from brain postmortem tissue

  Chart genetic variation in the human brain in healthy controls and Parkinson’s disease (PD) patients.

  Study EGAS50000000921

• ONT and PacBio data of 22q11 patient-parent duos/trios

  ONT and PacBio FASTQ files generated for de novo assembly and resulting de novo assemblies

  Study EGAS50000001647

• Myeloproliferative_Neoplasms__MPN__Exome_Validation_Study

  Experiments using targeted pulldown methods will be sequenced to validate findings in the exomes of patients with Myeloproliferative Neoplasms (MPN).

  Study EGAS00001000404

• ESGI___Whole_Genome_Sequencing_of_NSPHS_samples

  Whole genome sequencing of sampels from the NSPHS cohort. The samples are sequenced using the Illumina HiSeq X Ten system.

  Study EGAS00001001117