Pages that link to "Q25257750"
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The following pages link to BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH) (Q25257750):
Displaying 50 items.
- Array-CGH in patients with Kabuki-like phenotype: identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration (Q21261428) (← links)
- Global variation in copy number in the human genome (Q24658083) (← links)
- The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation (Q28685216) (← links)
- Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies (Q28752220) (← links)
- Flexible and accurate detection of genomic copy-number changes from aCGH. (Q30479616) (← links)
- Progenetix: 12 years of oncogenomic data curation (Q30694445) (← links)
- ACTuDB, a new database for the integrated analysis of array-CGH and clinical data for tumors. (Q31112364) (← links)
- ADaCGH: A parallelized web-based application and R package for the analysis of aCGH data (Q31122219) (← links)
- Normalization of array-CGH data: influence of copy number imbalances (Q31133934) (← links)
- wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data (Q31149372) (← links)
- Array-CGH and multipoint FISH to decode complex chromosomal rearrangements (Q33267915) (← links)
- Resolving the resolution of array CGH. (Q33271882) (← links)
- Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer. (Q33274761) (← links)
- A new look towards BAC-based array CGH through a comprehensive comparison with oligo-based array CGH. (Q33280495) (← links)
- Gene-resolution analysis of DNA copy number variation using oligonucleotide expression microarrays (Q33283252) (← links)
- Random DNA fragmentation allows detection of single-copy, single-exon alterations of copy number by oligonucleotide array CGH in clinical FFPE samples (Q33608830) (← links)
- Opening the archives for state of the art tumour genetic research: sample processing for array-CGH using decalcified, formalin-fixed, paraffin-embedded tissue-derived DNA samples (Q33785386) (← links)
- Absence/presence calling in microarray-based CGH experiments with non-model organisms (Q33791167) (← links)
- Highly parallel genomic assays (Q33997732) (← links)
- Array Comparative Genomic Hybridizations: assessing the ability to recapture evolutionary relationships using an in silico approach (Q34026815) (← links)
- Safety paradigm: genetic evaluation of therapeutic grade human embryonic stem cells (Q34333314) (← links)
- DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly (Q34590458) (← links)
- Genome-wide comparison of paired fresh frozen and formalin-fixed paraffin-embedded gliomas by custom BAC and oligonucleotide array comparative genomic hybridization: facilitating analysis of archival gliomas. (Q34687243) (← links)
- A robust method to analyze copy number alterations of less than 100 kb in single cells using oligonucleotide array CGH. (Q34794604) (← links)
- Detecting structural variations in the human genome using next generation sequencing (Q34831573) (← links)
- Similarity in genetic alterations between paired well-differentiated and dedifferentiated components of dedifferentiated liposarcoma (Q35001466) (← links)
- High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping (Q35012994) (← links)
- Accurate and reliable high-throughput detection of copy number variation in the human genome (Q35173713) (← links)
- Report of the EORTC-PAMM Meeting, Brussels, 16-18 March 2009: new strategies for a targeted and personalised therapy of cancer (Q35572921) (← links)
- Penalized weighted low-rank approximation for robust recovery of recurrent copy number variations (Q35864949) (← links)
- Preservation of skin DNA for oligonucleotide array CGH studies: a feasibility study (Q35945546) (← links)
- A Robust Protocol for Using Multiplexed Droplet Digital PCR to Quantify Somatic Copy Number Alterations in Clinical Tissue Specimens (Q36107089) (← links)
- Computational methods for the analysis of array comparative genomic hybridization. (Q36122880) (← links)
- A portrait of copy-number polymorphism in Drosophila melanogaster (Q36288935) (← links)
- CanGEM: mining gene copy number changes in cancer (Q36454366) (← links)
- Strategies for the detection of copy number and other structural variants in the human genome (Q36474973) (← links)
- PAIR: paired allelic log-intensity-ratio-based normalization method for SNP-CGH arrays. (Q36581062) (← links)
- Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues (Q36719179) (← links)
- Genome profiling of ovarian adenocarcinomas using pangenomic BACs microarray comparative genomic hybridization (Q36731272) (← links)
- Array comparative genomic hybridization analysis identifies recurrent gain of chromosome 2p25.3 involving the ACP1 and MYCN genes in chronic lymphocytic leukemia (Q36837347) (← links)
- Getting it right: designing microarray (and not 'microawry') comparative genomic hybridization studies for cancer research (Q36844700) (← links)
- Methods and strategies for analyzing copy number variation using DNA microarrays (Q36863499) (← links)
- Molecular cytogenetics: making it safe for human embryonic stem cells to enter the clinic (Q36874341) (← links)
- Characterization of breast cancer by array comparative genomic hybridization. (Q36916665) (← links)
- Detection of DNA copy number alterations in cancer by array comparative genomic hybridization (Q36943634) (← links)
- Oligonucleotide arrays for high-resolution analysis of copy number alteration in mental retardation/multiple congenital anomalies (Q36943647) (← links)
- Molecular diagnostic testing in malignant gliomas: a practical update on predictive markers (Q37037132) (← links)
- De novo complex intra chromosomal rearrangement after ICSI: characterisation by BACs micro array-CGH. (Q37130409) (← links)
- A single-sample method for normalizing and combining full-resolution copy numbers from multiple platforms, labs and analysis methods (Q37140342) (← links)
- From cytogenetics to next-generation sequencing technologies: advances in the detection of genome rearrangements in tumors (Q37149910) (← links)