1330 results for "comprar monedas FC mobile 26 Visité Buyfc26coins.com. ¡Impresionante! En menos de 15 minutos todo listo..4X8G"

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• Targeted capture ctDNA Library CRCQV42Run051-15

  Targeted capture ctDNA Library CRCQV42Run051-15 from patient PBC0001224, buffy coat sample

  Dataset EGAD00001010809

• Targeted capture ctDNA Library CRCQV42Run048-15

  Targeted capture ctDNA Library CRCQV42Run048-15 from patient PBC0001818, buffy coat sample

  Dataset EGAD00001010747

• Targeted capture ctDNA Library CRCQV42Run034-15

  Targeted capture ctDNA Library CRCQV42Run034-15 from patient PBC0004565, buffy coat sample

  Dataset EGAD00001010569

• Targeted capture ctDNA Library CRCQV42Run050-15

  Targeted capture ctDNA Library CRCQV42Run050-15 from patient PBC0001183, buffy coat sample

  Dataset EGAD00001010788

• Targeted capture ctDNA Library CRCQV34Run011-15

  Targeted capture ctDNA Library CRCQV34Run011-15 from patient PBC0002383, buffy coat sample

  Dataset EGAD00001010369

• Targeted capture ctDNA Library CRCQV42Run030-15

  Targeted capture ctDNA Library CRCQV42Run030-15 from patient PBC0003014, buffy coat sample

  Dataset EGAD00001010521

• Targeted capture ctDNA Library CRCQV42Run047-15

  Targeted capture ctDNA Library CRCQV42Run047-15 from patient PBC0002255, buffy coat sample

  Dataset EGAD00001010727

• Targeted capture ctDNA Library CRCQV42Run021-15

  Targeted capture ctDNA Library CRCQV42Run021-15 from patient PBC0001323, plasma baseline sample

  Dataset EGAD00001010437

• Targeted capture ctDNA Library CRCQV42Run049-15

  Targeted capture ctDNA Library CRCQV42Run049-15 from patient PBC0001782, buffy coat sample

  Dataset EGAD00001010768

• SweGen genetic variation from the Swedish Twin Registry

  The dataset contains files with single nucleotide variants in VCF format for a total of 942 DNA samples, selected to represent a cross-section of the Swedish population. The samples originate from the Swedish Twin Registry (STR) and have been obtained from different geographical regions. For each of the 942 individuals, DNA was extracted from a blood sample and subject to whole genome sequencing (WGS). The WGS was performed using 2x150 bp paired-end chemistry on Illumina HiSeq X Ten instrumentation at the SciLifeLab National Genomics Infrastructure (NGI) in Stockholm and Uppsala. FASTQ files generated by WGS were analyzed using the nf-core pipeline Sarek, which includes pre-processing, alignment to the human GRCh38 reference genome, and germline variant calling. All participants gave their written informed consent and the TwinGene study was approved by the regional ethics committee (Regionala Etikprövningsnämnden, Stockholm, dnr 2007-644-31, dnr 2014/521-32). Access to phenotypic information can be requested from the Swedish Twin Registry (http://ki.se/en/research/the-swedish-twin-registry).

  Dataset EGAD50000001323