| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1111/J.1541-0420.2009.01353.X |
| P932 | PMC publication ID | 2888717 |
| P698 | PubMed publication ID | 19912177 |
| P5875 | ResearchGate publication ID | 38088158 |
| P894 | zbMATH Open document ID | 1203.62182 |
| P50 | author | Rafael Irizarry | Q39073664 |
| Héctor Corrada Bravo | Q35703653 | ||
| P2860 | cites work | Toward the 1,000 dollars human genome. | Q36186955 |
| An estimate of the crosstalk matrix in four-dye fluorescence-based DNA sequencing | Q41682165 | ||
| International genome project launched. | Q53221818 | ||
| The death of microarrays? | Q59094468 | ||
| Ultrafast and memory-efficient alignment of short DNA sequences to the human genome | Q21183894 | ||
| Model-based analysis of ChIP-Seq (MACS) | Q21183902 | ||
| Mapping and quantifying mammalian transcriptomes by RNA-Seq | Q22122035 | ||
| Genome sequencing in microfabricated high-density picolitre reactors | Q24544260 | ||
| Genome-wide analysis of transcription factor binding sites based on ChIP-Seq data | Q24595121 | ||
| Genome-wide maps of chromatin state in pluripotent and lineage-committed cells | Q24632506 | ||
| Mapping short DNA sequencing reads and calling variants using mapping quality scores | Q24644612 | ||
| Application of massively parallel sequencing to microRNA profiling and discovery in human embryonic stem cells | Q24646863 | ||
| RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays | Q24655562 | ||
| Base-calling of automated sequencer traces using phred. I. Accuracy assessment | Q27860665 | ||
| A comparison of normalization methods for high density oligonucleotide array data based on variance and bias | Q27860710 | ||
| Accurate multiplex polony sequencing of an evolved bacterial genome | Q28265850 | ||
| An introduction to ROC analysis | Q29299877 | ||
| Substantial biases in ultra-short read data sets from high-throughput DNA sequencing | Q29617050 | ||
| Genome-wide identification of in vivo protein-DNA binding sites from ChIP-Seq data | Q31169616 | ||
| Probabilistic base calling of Solexa sequencing data | Q33375519 | ||
| An integrated software system for analyzing ChIP-chip and ChIP-seq data | Q33382059 | ||
| Alta-Cyclic: a self-optimizing base caller for next-generation sequencing | Q34299405 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P6104 | maintained by WikiProject | WikiProject Mathematics | Q8487137 |
| P304 | page(s) | 665-674 | |
| P577 | publication date | 2010-09-01 | |
| P1433 | published in | Biometrics | Q2025724 |
| P1476 | title | Model-based quality assessment and base-calling for second-generation sequencing data | |
| P478 | volume | 66 |
| Q34299351 | A platform-independent method for detecting errors in metagenomic sequencing data: DRISEE. |
| Q34179097 | All Your Base: a fast and accurate probabilistic approach to base calling |
| Q30586095 | BM-BC: a Bayesian method of base calling for Solexa sequence data |
| Q33881427 | BM-map: Bayesian mapping of multireads for next-generation sequencing data |
| Q21184009 | BSmooth: from whole genome bisulfite sequencing reads to differentially methylated regions |
| Q37829810 | Base-calling for next-generation sequencing platforms |
| Q30731247 | BlindCall: ultra-fast base-calling of high-throughput sequencing data by blind deconvolution |
| Q42672459 | CLEVER: clique-enumerating variant finder |
| Q37615067 | Characterization of the Genomic Diversity of Norovirus in Linked Patients Using a Metagenomic Deep Sequencing Approach |
| Q34487751 | Commentary: Call for a Quality Standard for Sequence-Based Assays in Clinical Microbiology: Necessity for Quality Assessment of Sequences Used in Microbial Identification and Typing |
| Q28748746 | Development of a low bias method for characterizing viral populations using next generation sequencing technology |
| Q42102818 | Effective detection of rare variants in pooled DNA samples using Cross-pool tailcurve analysis |
| Q28713966 | Estimation of sequencing error rates in short reads |
| Q34096126 | Family-based association tests using genotype data with uncertainty |
| Q38249872 | Identifying and mitigating bias in next-generation sequencing methods for chromatin biology |
| Q34476783 | Improved base-calling and quality scores for 454 sequencing based on a Hurdle Poisson model |
| Q42838840 | Intensity normalization improves color calling in SOLiD sequencing |
| Q59351138 | Inter- and Intra-Host Nucleotide Variations in Hepatitis A Virus in Culture and Clinical Samples Detected by Next-Generation Sequencing |
| Q48444711 | John Storey by Mak H Craig |
| Q34314953 | MetaMicrobesOnline: phylogenomic analysis of microbial communities |
| Q38061737 | Next-generation sequencing in the clinic: promises and challenges |
| Q30720610 | Oligotyping: Differentiating between closely related microbial taxa using 16S rRNA gene data. |
| Q33767163 | Overcoming bias and systematic errors in next generation sequencing data |
| Q35167233 | Quake: quality-aware detection and correction of sequencing errors |
| Q34580821 | Robust Detection and Identification of Sparse Segments in Ultra-High Dimensional Data Analysis |
| Q34964688 | Searching for SNPs with cloud computing |
| Q34354210 | Short-read reading-frame predictors are not created equal: sequence error causes loss of signal |
| Q41863570 | Simultaneous mapping of multiple gene loci with pooled segregants |
| Q33757432 | Statistical Analyses of Next Generation Sequence Data: A Partial Overview |
| Q28728245 | Summarizing and correcting the GC content bias in high-throughput sequencing |
| Q91968519 | Systematic evaluation of library preparation methods and sequencing platforms for high-throughput whole genome bisulfite sequencing |
| Q30936152 | ViVaMBC: estimating viral sequence variation in complex populations from illumina deep-sequencing data using model-based clustering |
| Q33641952 | Visualization and probability-based scoring of structural variants within repetitive sequences |
| Q35780165 | pre-miRNA profiles obtained through application of locked nucleic acids and deep sequencing reveals complex 5'/3' arm variation including concomitant cleavage and polyuridylation patterns |
Search more.