Number of chromosomes, Feugen-DNA content, and nuclear phe- notypes in domestic and wild specimens of Panstrongylus megistus. Ann. Trop. Med. Parasitol. 80(6): 641Ð 648.Mello MLS, Randi MAF, Giorgio S, Ferraz-Filho AN, Rodrigues VLCC, Rocha-e-Silva EO, Cordeiro JA 1986. Number ...
Array comparative genomic hybridization (aCGH) is a newly introduced method for the detection of copy number abnormalities associated with human diseases with special focus on cancer. Specific patterns in DNA copy number variations (CNVs) can be associated with certain disease types and can facilitate...
Mutations in the SRY gene encompassing the HMG box have been well characterized in gonadal dysgenesis, male infertility and other types of sex chromosome related anomalies (SCRA). However, no information is available on copy number status of this gene under such abnormal conditions. Employing 'Taqma...
registered that year, 476 (78.9%) were submitted during the first 10 weeks after the disaster. Friction ridge analysis accounted for 67.9% of primary identifications and DNA analysis did so for 91.6% of re-identification cases....
The locus-specific mutation frequencies for copy number variation and other structural changes are two to four orders of magnitude greater than for point mutations. HR mechanisms generally achieve accurate repair of DNA damage. Double-stranded breaks are repaired by HR or by end-joining mechanisms, ...
Patterned self-assembly tile set synthesis (pats) aims at minimizing the number of distinct DNA tile types used to self-assemble a given rectangular color ... A Johnsen,MY Kao,S Seki - 《Journal of Combinatorial Optimization》 被引量: 1发表: 2017年 A secure data sharing using identity-based...
The two segments were significantly different with respect to the frequency of transcriptional units, the types and numbers of repetitive elements present, their GC content, and the number of CpG islands. Alu elements, GC content, and CpG islands all showed positive correlations with the abundance...
AmpliconSuite can also be run through Nextflow, using thenf-core/circdna pipelineconstructed byDaniel Schreyer. Installation AA can be installed in three ways: Conda installation of AmpliconSuite-pipeline (which includes AA and all recommended modules). ...
Cells of these different nucleolar types, however, contained essentially the same amount of rDNA (DNA complementary to rRNA) as estimated by in situ hybridization with [ 125I]rRNA. Although it remains to be proved that the observed increase in incorporation represents the increased rate of rRNA ...
The goal of epiAneufinder is to segment the genome into regions of gain, loss, and normal copy number per single cell. To do that, epiAneufinder uses the number of reads from scATAC-seq data mapping to a genomic region as a proxy of the number of DNA copies present in that region, ...