Sentence examples for based on available genomic from inspiring English sources

PCR product size was predicted to be 608 bp based on available genomic data for the B6 reference strain.

Based on available genomic sequences of humans and a number of primates, an evolutionary analysis was conducted in the present study comparing human and non-human primate sequences in the schizophrenia-associated GABRB2 region in order to detect any sequence signatures of human-lineage specific changes that could be indicative of natural selection and therefore functional significance.

To obtain an evaluation dataset, we constructed a PCUE (Predicted genes, FL- cDNA, UniGene, and EST) database based on available genomic resources (see Materials and Methods).

Their lack of identity based on available genomic and EST resources could mean that the non-annotated cDNAs contain incomplete sequence information for orthologous matches with other databases.

The AtWRI1 from embryo as well as the two homologs from potato and poplar were synthetically ordered (Eurofins, Ebersberg, Germany) based on available genomic resources.

Specific primers for each gene were designed based on available genomic or cDNA sequences and on the alignment with related genes to avoid cross-amplification, using Beacon Design software (Premier Biosoft Int., Palo Alto, CA).

Based on available genetic maps, it is then necessary to select the appropriate genotype(s) from which to develop supporting genomic resources.

A phylogenetic analysis based on available full-length genomic PEDV sequences indicated that all PEDV strains were classified into 2 distinct genogroups: G1 and G2 (6 ).

Cichlid-specific PCR primers were designed based on available and/or draft genomic and transcriptomic cichlid sequences, which were identified by tblastx searches of publicly available dlx sequences from other teleost species (see Additional file 1 for species and accession numbers).

We suggest a testing algorithm to identify genomic variation in clinical samples based on available technologies for mutation detection and the clinical presentation of the patient.

For each case, a population of genomic regions affected by copy number gain was identified based on available karyotyping data.