Pages that link to "Q42558307"
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The following pages link to Improved base calling for the Illumina Genome Analyzer using machine learning strategies (Q42558307):
Displaying 50 items.
- Unexplored character diversity in onychophora (velvet worms): A comparative study of three peripatid species (Q21133998) (← links)
- Whole mitochondrial genome sequencing of domestic horses reveals incorporation of extensive wild horse diversity during domestication (Q21284046) (← links)
- A Draft Sequence of the Neandertal Genome (Q22065895) (← links)
- Genetic history of an archaic hominin group from Denisova Cave in Siberia (Q22122173) (← links)
- The complete mitochondrial DNA genome of an unknown hominin from southern Siberia (Q22122180) (← links)
- Targeted enrichment of ancient pathogens yielding the pPCP1 plasmid of Yersinia pestis from victims of the Black Death (Q22248082) (← links)
- Denisova admixture and the first modern human dispersals into Southeast Asia and Oceania (Q22252551) (← links)
- Genome sequence of a 45,000-year-old modern human from western Siberia (Q24205724) (← links)
- A high-coverage genome sequence from an archaic Denisovan individual (Q24595378) (← links)
- IPED: a highly efficient denoising tool for Illumina MiSeq Paired-end 16S rRNA gene amplicon sequencing data (Q27319083) (← links)
- A comparison of brain gene expression levels in domesticated and wild animals (Q27331419) (← links)
- High-throughput RNA sequencing of a formalin-fixed, paraffin-embedded autopsy lung tissue sample from the 1918 influenza pandemic (Q28279911) (← links)
- Complete mitochondrial genomes of ancient canids suggest a European origin of domestic dogs (Q28301981) (← links)
- The complete genome sequence of a Neanderthal from the Altai Mountains (Q28304347) (← links)
- MACSE: Multiple Alignment of Coding SEquences accounting for frameshifts and stop codons (Q28334425) (← links)
- Reference-Free Validation of Short Read Data (Q28475554) (← links)
- Ligation bias in illumina next-generation DNA libraries: implications for sequencing ancient genomes (Q28534717) (← links)
- First ancient mitochondrial human genome from a prepastoralist southern African (Q28652549) (← links)
- Separating endogenous ancient DNA from modern day contamination in a Siberian Neandertal (Q28659012) (← links)
- Complete mtDNA genomes of Filipino ethnolinguistic groups: a melting pot of recent and ancient lineages in the Asia-Pacific region (Q28660510) (← links)
- RNAseq versus genome-predicted transcriptomes: a large population of novel transcripts identified in an Illumina-454 Hydra transcriptome (Q28681183) (← links)
- Next-generation museomics disentangles one of the largest primate radiations (Q28681692) (← links)
- Challenges and opportunities in estimating viral genetic diversity from next-generation sequencing data (Q28727944) (← links)
- High-throughput sequencing of complete human mtDNA genomes from the Caucasus and West Asia: high diversity and demographic inferences (Q28744619) (← links)
- The evolution of gene expression levels in mammalian organs (Q29617170) (← links)
- Genetic influences on brain gene expression in rats selected for tameness and aggression (Q30399799) (← links)
- Inferring the evolutionary histories of divergences in Hylobates and Nomascus gibbons through multilocus sequence data (Q30455201) (← links)
- BM-BC: a Bayesian method of base calling for Solexa sequence data (Q30586095) (← links)
- Identification of optimum sequencing depth especially for de novo genome assembly of small genomes using next generation sequencing data (Q30617713) (← links)
- BlindCall: ultra-fast base-calling of high-throughput sequencing data by blind deconvolution (Q30731247) (← links)
- Estimating genotype error rates from high-coverage next-generation sequence data (Q30859169) (← links)
- CRCDA--Comprehensive resources for cancer NGS data analysis (Q31003638) (← links)
- An NGS Workflow Blueprint for DNA Sequencing Data and Its Application in Individualized Molecular Oncology. (Q31077769) (← links)
- Synthetic spike-in standards improve run-specific systematic error analysis for DNA and RNA sequencing (Q31079862) (← links)
- From next-generation resequencing reads to a high-quality variant data set. (Q31137675) (← links)
- Visualization and probability-based scoring of structural variants within repetitive sequences (Q33641952) (← links)
- Analysis of plant microbe interactions in the era of next generation sequencing technologies (Q33659736) (← links)
- MOIRAI: a compact workflow system for CAGE analysis (Q33662599) (← links)
- Multiplexed DNA sequence capture of mitochondrial genomes using PCR products (Q33754699) (← links)
- Statistical Analyses of Next Generation Sequence Data: A Partial Overview (Q33757432) (← links)
- From reads to operational taxonomic units: an ensemble processing pipeline for MiSeq amplicon sequencing data (Q33784861) (← links)
- Detection and removal of biases in the analysis of next-generation sequencing reads (Q33815482) (← links)
- Computational Analysis of High Throughput Sequencing Data (Q33836085) (← links)
- Genotype and SNP calling from next-generation sequencing data (Q33903792) (← links)
- Transmission from centenarians to their offspring of mtDNA heteroplasmy revealed by ultra-deep sequencing (Q33910477) (← links)
- Addressing challenges in the production and analysis of illumina sequencing data (Q33975605) (← links)
- Double indexing overcomes inaccuracies in multiplex sequencing on the Illumina platform (Q34054922) (← links)
- Comparative analysis of functional metagenomic annotation and the mappability of short reads (Q34078749) (← links)
- The genomic architecture of population divergence between subspecies of the European rabbit (Q34104420) (← links)
- COLD-PCR enrichment of rare cancer mutations prior to targeted amplicon resequencing (Q34109720) (← links)