Pages that link to "Q36480006"
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The following pages link to CREST maps somatic structural variation in cancer genomes with base-pair resolution. (Q36480006):
Displaying 50 items.
- COPS: a sensitive and accurate tool for detecting somatic Copy Number Alterations using short-read sequence data from paired samples (Q21133928) (← links)
- LUMPY: a probabilistic framework for structural variant discovery. (Q21999523) (← links)
- The genetic basis of early T-cell precursor acute lymphoblastic leukaemia (Q24601515) (← links)
- Using ERDS to infer copy-number variants in high-coverage genomes (Q24604693) (← links)
- DELLY: structural variant discovery by integrated paired-end and split-read analysis (Q24605418) (← links)
- Integrated analysis of whole-genome paired-end and mate-pair sequencing data for identifying genomic structural variations in multiple myeloma (Q26829846) (← links)
- Genomic profiling of B-progenitor acute lymphoblastic leukemia (Q26829976) (← links)
- Legume genomics: understanding biology through DNA and RNA sequencing (Q26849760) (← links)
- Structural variation discovery in the cancer genome using next generation sequencing: computational solutions and perspectives (Q26991436) (← links)
- Recurrent BRAF kinase fusions in melanocytic tumors offer an opportunity for targeted therapy (Q27852482) (← links)
- Detection of Genomic Structural Variants from Next-Generation Sequencing Data (Q28082859) (← links)
- PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data (Q28383251) (← links)
- A genome-wide approach for detecting novel insertion-deletion variants of mid-range size (Q28388359) (← links)
- Common Oncogene Mutations and Novel SND1-BRAF Transcript Fusion in Lung Adenocarcinoma from Never Smokers (Q28394324) (← links)
- Getting personalized cancer genome analysis into the clinic: the challenges in bioinformatics (Q28394818) (← links)
- Evolution of multiple cell clones over a 29-year period of a CLL patient (Q28396836) (← links)
- Elucidating emergence and transmission of multidrug-resistant tuberculosis in treatment experienced patients by whole genome sequencing (Q28536869) (← links)
- Whole genome sequencing based characterization of extensively drug-resistant Mycobacterium tuberculosis isolates from Pakistan (Q28543682) (← links)
- Fitness consequences of polymorphic inversions in the zebra finch genome (Q28598120) (← links)
- Bionimbus: a cloud for managing, analyzing and sharing large genomics datasets (Q28652892) (← links)
- Bellerophon: a hybrid method for detecting interchromosomal rearrangements at base pair resolution using next-generation sequencing data (Q29584348) (← links)
- CONSERTING: integrating copy-number analysis with structural-variation detection (Q30397544) (← links)
- SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay (Q30566015) (← links)
- A survey of copy-number variation detection tools based on high-throughput sequencing data. (Q30573762) (← links)
- Assessing telomeric DNA content in pediatric cancers using whole-genome sequencing data (Q30581144) (← links)
- SOAPfuse: an algorithm for identifying fusion transcripts from paired-end RNA-Seq data (Q30588697) (← links)
- VirusFinder: software for efficient and accurate detection of viruses and their integration sites in host genomes through next generation sequencing data (Q30635438) (← links)
- A genomic random interval model for statistical analysis of genomic lesion data (Q30654515) (← links)
- SV-AUTOPILOT: optimized, automated construction of structural variation discovery and benchmarking pipelines. (Q30659544) (← links)
- Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches (Q30729747) (← links)
- Population genetic analysis of bi-allelic structural variants from low-coverage sequence data with an expectation-maximization algorithm (Q30828106) (← links)
- BSSV: Bayesian based somatic structural variation identification with whole genome DNA-seq data (Q30883476) (← links)
- Methods for the detection and assembly of novel sequence in high-throughput sequencing data (Q30887428) (← links)
- Identification of copy number variants in whole-genome data using Reference Coverage Profiles (Q30904066) (← links)
- INTEGRATE: gene fusion discovery using whole genome and transcriptome data (Q31021342) (← links)
- SAAS-CNV: A Joint Segmentation Approach on Aggregated and Allele Specific Signals for the Identification of Somatic Copy Number Alterations with Next-Generation Sequencing Data (Q31026307) (← links)
- Analysis of genomic rearrangements by using the Burrows-Wheeler transform of short-read data (Q31032614) (← links)
- Sprites: detection of deletions from sequencing data by re-aligning split reads (Q31041990) (← links)
- Structural variation detection using next-generation sequencing data: A comparative technical review. (Q31043037) (← links)
- Identification of Known and Novel Recurrent Viral Sequences in Data from Multiple Patients and Multiple Cancers (Q31048577) (← links)
- Discovering and understanding oncogenic gene fusions through data intensive computational approaches (Q31083417) (← links)
- MOSAIK: a hash-based algorithm for accurate next-generation sequencing short-read mapping (Q31153287) (← links)
- Germline ETV6 Mutations Confer Susceptibility to Acute Lymphoblastic Leukemia and Thrombocytopenia (Q33423823) (← links)
- digit-a tool for detection and identification of genomic interchromosomal translocations (Q33701551) (← links)
- C11orf95-RELA fusions drive oncogenic NF-κB signalling in ependymoma (Q33730977) (← links)
- Tumor haplotype assembly algorithms for cancer genomics (Q33732433) (← links)
- BreakTrans: uncovering the genomic architecture of gene fusions (Q33744985) (← links)
- The genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade glioma (Q33751426) (← links)
- PolyTB: a genomic variation map for Mycobacterium tuberculosis (Q33791955) (← links)
- The most informative spacing test effectively discovers biologically relevant outliers or multiple modes in expression (Q33796443) (← links)