Pages that link to "Q28728245"
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The following pages link to Summarizing and correcting the GC content bias in high-throughput sequencing (Q28728245):
Displaying 50 items.
- GROM-RD: resolving genomic biases to improve read depth detection of copy number variants (Q21128696) (← links)
- Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement (Q21183963) (← links)
- An improved genome of the model marine alga Ostreococcus tauri unfolds by assessing Illumina de novo assemblies (Q21266653) (← links)
- The fast changing landscape of sequencing technologies and their impact on microbial genome assemblies and annotation (Q21560744) (← links)
- IVT-seq reveals extreme bias in RNA sequencing (Q21999522) (← links)
- Harnessing the power of RADseq for ecological and evolutionary genomics (Q26771227) (← links)
- Can all heritable biology really be reduced to a single dimension? (Q26771372) (← links)
- Differential Expression Analysis for RNA-Seq: An Overview of Statistical Methods and Computational Software (Q26774631) (← links)
- Microarray experiments and factors which affect their reliability (Q26786123) (← links)
- Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges (Q26864808) (← links)
- Chromothripsis from DNA damage in micronuclei. (Q27316519) (← links)
- Toward Accurate and Quantitative Comparative Metagenomics (Q28076421) (← links)
- Protein-DNA binding in high-resolution (Q28084330) (← links)
- A High-Coverage Yersinia pestis Genome from a Sixth-Century Justinianic Plague Victim (Q28137475) (← links)
- The statistical-mechanics of chromosome conformation capture (Q28298852) (← links)
- Systematic biases in DNA copy number originate from isolation procedures (Q28387704) (← links)
- A genome-wide approach for detecting novel insertion-deletion variants of mid-range size (Q28388359) (← links)
- Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease (Q28509829) (← links)
- Ligation bias in illumina next-generation DNA libraries: implications for sequencing ancient genomes (Q28534717) (← links)
- HCV genotyping from NGS short reads and its application in genotype detection from HCV mixed infected plasma (Q28545256) (← links)
- Fast, Accurate and Automatic Ancient Nucleosome and Methylation Maps with epiPALEOMIX (Q28596169) (← links)
- Izumo1 and Juno: the evolutionary origins and coevolution of essential sperm-egg binding partners (Q28601974) (← links)
- Understanding spatial organizations of chromosomes via statistical analysis of Hi-C data (Q28647858) (← links)
- Genome-wide nucleosome map and cytosine methylation levels of an ancient human genome (Q28658266) (← links)
- Comparison of three next-generation sequencing platforms for metagenomic sequencing and identification of pathogens in blood. (Q30358677) (← links)
- Pattern Recognition on Read Positioning in Next Generation Sequencing. (Q30378821) (← links)
- Impact of library preparation protocols and template quantity on the metagenomic reconstruction of a mock microbial community (Q30400521) (← links)
- Non-random DNA fragmentation in next-generation sequencing. (Q30440990) (← links)
- Sequencing platform and library preparation choices impact viral metagenomes (Q30454551) (← links)
- Comparative RNA-Seq and microarray analysis of gene expression changes in B-cell lymphomas of Canis familiaris. (Q30455450) (← links)
- Special features of RAD Sequencing data: implications for genotyping (Q30575346) (← links)
- RNase L targets distinct sites in influenza A virus RNAs. (Q30620296) (← links)
- Effects of GC bias in next-generation-sequencing data on de novo genome assembly (Q30620847) (← links)
- Characterizing and measuring bias in sequence data (Q30635784) (← links)
- Estimating exome genotyping accuracy by comparing to data from large scale sequencing projects (Q30658414) (← links)
- HMCan: a method for detecting chromatin modifications in cancer samples using ChIP-seq data. (Q30666001) (← links)
- Statistical and Computational Methods for High-Throughput Sequencing Data Analysis of Alternative Splicing (Q30668937) (← links)
- Comparative studies of differential gene calling using RNA-Seq data (Q30699743) (← links)
- Next-generation technologies and data analytical approaches for epigenomics (Q30712646) (← links)
- Evaluation of assembly strategies using RNA-seq data associated with grain development of wheat (Triticum aestivum L.). (Q30717960) (← links)
- Oligotyping: Differentiating between closely related microbial taxa using 16S rRNA gene data. (Q30720610) (← links)
- Prevention, diagnosis and treatment of high-throughput sequencing data pathologies (Q30743735) (← links)
- Reducing bias in RNA sequencing data: a novel approach to compute counts (Q30763179) (← links)
- Adaptive bandwidth kernel density estimation for next-generation sequencing data (Q30763407) (← links)
- Integrative RNA-seq and microarray data analysis reveals GC content and gene length biases in the psoriasis transcriptome (Q30824606) (← links)
- Detecting and correcting systematic variation in large-scale RNA sequencing data (Q30844399) (← links)
- cnvCapSeq: detecting copy number variation in long-range targeted resequencing data. (Q30852238) (← links)
- Measuring differential gene expression with RNA-seq: challenges and strategies for data analysis (Q30853974) (← links)
- BADGE: a novel Bayesian model for accurate abundance quantification and differential analysis of RNA-Seq data. (Q30855028) (← links)
- Quantifying tumor heterogeneity in whole-genome and whole-exome sequencing data (Q30858364) (← links)