Pages that link to "Q34403997"

The following pages link to A mechanistic basis for amplification differences between samples and between genome regions (Q34403997):

Displaying 24 items.

• Navigating the rapids: the development of regulated next-generation sequencing-based clinical trial assays and companion diagnostics (Q26864332) (← links)
• Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation (Q28263098) (← links)
• Systematic biases in DNA copy number originate from isolation procedures (Q28387704) (← links)
• The Use of Non-Variant Sites to Improve the Clinical Assessment of Whole-Genome Sequence Data (Q30978835) (← links)
• Simultaneous human platelet antigen genotyping and detection of novel single nucleotide polymorphisms by targeted next-generation sequencing (Q33440638) (← links)
• Synthetic spike-in standards for high-throughput 16S rRNA gene amplicon sequencing (Q33557389) (← links)
• Obesity, starch digestion and amylase: association between copy number variants at human salivary (AMY1) and pancreatic (AMY2) amylase genes (Q34043497) (← links)
• Sequencing depth and coverage: key considerations in genomic analyses (Q34398440) (← links)
• Accurate measurement of gene copy number for human alpha-defensin DEFA1A3. (Q35020478) (← links)
• Variant detection sensitivity and biases in whole genome and exome sequencing (Q35209205) (← links)
• Evaluation of High-Throughput Genomic Assays for the Fc Gamma Receptor Locus. (Q35834551) (← links)
• Molecular Detection of 10 of the Most Unwanted Alien Forest Pathogens in Canada Using Real-Time PCR. (Q35956116) (← links)
• Computational identification of putative lincRNAs in mouse embryonic stem cell (Q37319710) (← links)
• Multi-template polymerase chain reaction (Q37433707) (← links)
• A 129-kb deletion on chromosome 12 confers substantial protection against rheumatoid arthritis, implicating the gene SLC2A3. (Q37715658) (← links)
• New technologies for DNA analysis--a review of the READNA Project (Q38619509) (← links)
• Exome Sequencing: Current and Future Perspectives (Q38988654) (← links)
• Analysis of Copy Number Variation Using the Paralogue Ratio Test (PRT). (Q39002354) (← links)
• Sample tracking in microbiome community profiling assays using synthetic 16S rRNA gene spike-in controls. (Q55290469) (← links)
• Comparison of whole-genome (13X) and capture (87X) resequencing methods for SNP and genotype callings (Q57764652) (← links)
• Akkermansia muciniphila as a Model Case for the Development of an Improved Quantitative RPA Microbiome Assay (Q90542795) (← links)
• The kinetic requirements of extreme qPCR (Q91726903) (← links)
• Bioinformatics Strategies, Challenges, and Opportunities for Next Generation Sequencing-Based HLA Genotyping (Q91936174) (← links)
• Next-generation sequencing of newborn screening genes: the accuracy of short-read mapping (Q99565801) (← links)