Pages that link to "Q35798265"

The following pages link to Evaluation of the Illumina(®) Beta Version ForenSeq™ DNA Signature Prep Kit for use in genetic profiling (Q35798265):

Displaying 41 items.

• Effects of the Ion PGM™ Hi-Q™ sequencing chemistry on sequence data quality (Q31064721) (← links)
• A SNP panel for identity and kinship testing using massive parallel sequencing (Q38632477) (← links)
• Massively parallel sequencing of customised forensically informative SNP panels on the MiSeq (Q36125877) (← links)
• Forensically relevant SNaPshot® assays for human DNA SNP analysis: a review (Q36191391) (← links)
• Comparison between magnetic bead and qPCR library normalisation methods for forensic MPS genotyping (Q36349253) (← links)
• A technique for setting analytical thresholds in massively parallel sequencing-based forensic DNA analysis (Q36380417) (← links)
• Investigation of the STR loci noise distributions of PowerSeq™ Auto System. (Q38726197) (← links)
• The Y chromosomes of the great apes (Q38749896) (← links)
• Performance of the ForenSeqTM DNA Signature Prep kit on highly degraded samples. (Q39025524) (← links)
• Increasing the reach of forensic genetics with massively parallel sequencing (Q39385024) (← links)
• Case report: on the use of the HID-Ion AmpliSeq™ Ancestry Panel in a real forensic case (Q39548128) (← links)
• Empirical testing of a 23-AIMs panel of SNPs for ancestry evaluations in four major US populations (Q39968920) (← links)
• A panel of 130 autosomal single-nucleotide polymorphisms for ancestry assignment in five Asian populations and in Caucasians. (Q40229272) (← links)
• Comparison of Two Massively Parallel Sequencing Platforms using 83 Single Nucleotide Polymorphisms for Human Identification. (Q42061135) (← links)
• Qualitative and quantitative assessment of Illumina's forensic STR and SNP kits on MiSeq FGx™. (Q47096123) (← links)
• An assessment of a massively parallel sequencing approach for the identification of individuals from mass graves of the Spanish Civil War (1936-1939). (Q47260668) (← links)
• As solid as a rock-comparison of CE- and MPS-based analyses of the petrosal bone as a source of DNA for forensic identification of challenging cranial bones (Q47310136) (← links)
• A preliminary assessment of the ForenSeq™ FGx System: next generation sequencing of an STR and SNP multiplex. (Q47853722) (← links)
• Comparative tolerance of two massively parallel sequencing systems to common PCR inhibitors (Q49691142) (← links)
• A phylogenetic framework facilitates Y-STR variant discovery and classification via massively parallel sequencing. (Q52572709) (← links)
• Systematic assessment of the performance of illumina's MiSeq FGx™ forensic genomics system. (Q53636504) (← links)
• Analysis of four PCR/SNaPshot multiplex assays analyzing 52 SNPforID markers. (Q54134020) (← links)
• Genome-wide screen for universal individual identification SNPs based on the HapMap and 1000 Genomes databases. (Q54973971) (← links)
• TIA: algorithms for development of identity-linked SNP islands for analysis by massively parallel DNA sequencing. (Q55372431) (← links)
• Massively parallel sequencing analysis of nondegraded and degraded DNA mixtures using the ForenSeq™ system in combination with EuroForMix software (Q58103530) (← links)
• Massively parallel sequencing of 231 autosomal SNPs with a custom panel: a SNP typing assay developed for human identification with Ion Torrent PGM (Q58642223) (← links)
• Global patterns of STR sequence variation: Sequencing the CEPH human genome diversity panel for 58 forensic STRs using the Illumina ForenSeq DNA Signature Prep Kit (Q60296926) (← links)
• Short tandem repeat stutter model inferred from direct measurement of in vitro stutter noise (Q64254969) (← links)
• Current state-of-art of STR sequencing in forensic genetics (Q88639625) (← links)
• DNA identification of compromised samples with massive parallel sequencing (Q89458630) (← links)
• Evaluation of the performance of Illumina's ForenSeq™ system on serially degraded samples (Q90226338) (← links)
• An automated independent workflow for the analysis of massively parallel sequence data from forensic SNP assays (Q90232199) (← links)
• Massive parallel sequencing of short tandem repeats in the Korean population (Q90801259) (← links)
• Development of a SNP panel for predicting biogeographical ancestry and phenotype using massively parallel sequencing (Q90851227) (← links)
• Massively parallel sequencing techniques for forensics: A review (Q90913015) (← links)
• Human short tandem repeat identification using a nanopore-based DNA sequencer: a pilot study (Q90929751) (← links)
• Evaluation of ForenSeq™ Signature Prep Kit B on predicting eye and hair coloration as well as biogeographical ancestry by using Universal Analysis Software (UAS) and available web-tools (Q91607717) (← links)
• Characterization of sequence variation at 30 autosomal STRs in Chinese Han and Tibetan populations (Q92509094) (← links)
• Optimizing DNA recovery and forensic typing of degraded blood and dental remains using a specialized extraction method, comprehensive qPCR sample characterization, and massively parallel sequencing (Q92630253) (← links)
• Identification of sequence polymorphisms at 58 STRs and 94 iiSNPs in a Tibetan population using massively parallel sequencing (Q97652868) (← links)
• A set of novel multi-allelic SNPs for forensic application developed through massively parallel sequencing and its examples of population genetic studies (Q98730604) (← links)