Pages that link to "Q83337530"
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The following pages link to Single-cell chromosomal imbalances detection by array CGH (Q83337530):
Displaying 50 items.
- Specific and complete human genome amplification with improved yield achieved by phi29 DNA polymerase and a novel primer at elevated temperature (Q21202149) (← links)
- High-throughput sequencing for biology and medicine (Q26823498) (← links)
- Methods for comprehensive chromosome screening of oocytes and embryos: capabilities, limitations, and evidence of validity (Q26824853) (← links)
- Preimplantation genetic diagnosis (PGD) according to medical ethics and medical law (Q26862301) (← links)
- Chromosomal disorders and male infertility (Q26864151) (← links)
- Human molecular cytogenetics: From cells to nucleotides (Q27024633) (← links)
- An experimental loop design for the detection of constitutional chromosomal aberrations by array CGH. (Q30898664) (← links)
- High resolution array-CGH analysis of single cells (Q33267061) (← links)
- Detection of chromosomal structural alterations in single cells by SNP arrays: a systematic survey of amplification bias and optimized workflow (Q33309953) (← links)
- Single-cell isolation from cell suspensions and whole genome amplification from single cells to provide templates for CGH analysis (Q33310279) (← links)
- Effects of aneuploidy on genome structure, expression, and interphase organization in Arabidopsis thaliana (Q33377464) (← links)
- Molecular cytogenetics and cytogenomics of brain diseases (Q33464340) (← links)
- Human interphase chromosomes: a review of available molecular cytogenetic technologies. (Q33698277) (← links)
- Preclinical validation of a microarray method for full molecular karyotyping of blastomeres in a 24-h protocol (Q33731973) (← links)
- An algorithm for determining the origin of trisomy and the positions of chiasmata from SNP genotype data (Q33790894) (← links)
- The future of prenatal cytogenetic diagnostics: a personal perspective (Q33945745) (← links)
- Tracing the tumor lineage (Q33998432) (← links)
- Preimplantation genetic diagnosis: State of the ART 2011 (Q34199663) (← links)
- Origins and rates of aneuploidy in human blastomeres (Q34242703) (← links)
- Characterization of whole genome amplified (WGA) DNA for use in genotyping assay development (Q34289301) (← links)
- Singling out genetic disorders and disease (Q34334104) (← links)
- Whole genome amplification in preimplantation genetic diagnosis (Q34473168) (← links)
- Whole-genome multiple displacement amplification from single cells (Q34626413) (← links)
- Array comparative genomic hybridization analyses of all blastomeres of a cohort of embryos from young IVF patients revealed significant contribution of mitotic errors to embryo mosaicism at the cleavage stage (Q34636041) (← links)
- Guidelines for molecular karyotyping in constitutional genetic diagnosis (Q34653075) (← links)
- A robust method to analyze copy number alterations of less than 100 kb in single cells using oligonucleotide array CGH. (Q34794604) (← links)
- Morphokinetic analysis of cleavage stage embryos and its relationship to aneuploidy in a retrospective time-lapse imaging study (Q34962670) (← links)
- Direct squencing from the minimal number of DNA molecules needed to fill a 454 picotiterplate (Q35179729) (← links)
- Direct mutation analysis by high-throughput sequencing: from germline to low-abundant, somatic variants (Q35613426) (← links)
- Single-cell copy number variation detection. (Q35632586) (← links)
- Concurrent whole-genome haplotyping and copy-number profiling of single cells (Q35759080) (← links)
- New array approaches to explore single cells genomes (Q35887436) (← links)
- SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations (Q36170424) (← links)
- Preimplantation genetic diagnosis for aneuploidy and translocations using array comparative genomic hybridization. (Q36186429) (← links)
- Single cell genomics of the brain: focus on neuronal diversity and neuropsychiatric diseases. (Q36186434) (← links)
- Preimplantation genetic diagnosis: present and future (Q36268468) (← links)
- Current analysis platforms and methods for detecting copy number variation (Q36530874) (← links)
- High-resolution array comparative genomic hybridization of single micrometastatic tumor cells. (Q36633194) (← links)
- A procedure for highly specific, sensitive, and unbiased whole-genome amplification (Q36926786) (← links)
- Comprehensive chromosome analysis of blastocysts before implantation using array CGH. (Q37037926) (← links)
- Use of comprehensive chromosomal screening for embryo assessment: microarrays and CGH. (Q37091050) (← links)
- Identification of small gains and losses in single cells after whole genome amplification on tiling oligo arrays (Q37318486) (← links)
- Reliable single cell array CGH for clinical samples (Q37499802) (← links)
- Preimplantation genetic diagnosis guided by single-cell genomics (Q37691155) (← links)
- Preimplantation genetic testing: indications and controversies (Q37718643) (← links)
- Characterising chromosome rearrangements: recent technical advances in molecular cytogenetics (Q37956503) (← links)
- Prenatal and pre-implantation genetic diagnosis (Q38954748) (← links)
- Microarray analysis of copy number variation in single cells. (Q39409455) (← links)
- Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses (Q39617282) (← links)
- Evaluation of genome coverage and fidelity of multiple displacement amplification from single cells by SNP array (Q39813953) (← links)