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Transcriptional start sites of the GATA4 gene were mapped by rapid amplification of cDNA ends (5' RACE) using the GeneRacer kit according to instructions supplied by the manufacturer (Invitrogen).
Two of the three human FANTOM5 promoters associated with the human FABP4 gene were mapped in the coding region of the pig PMP2.
Homozygous deletions were observed at the locus where clones (9p21) containing the MTAP gene and CDKN2B (p16) gene were mapped in eight tumours of two patients, whereas high-level amplifications were not detected.
Antisense (AS) reads from the RNA-seq that fell within the annotated regions of each gene were mapped from both time points (T0 and T1) and antisense RPKM (Reads Per Kilobase of gene model per Million mapped reads) values were calculated.
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The gene was mapped to human chromosome 4q26 q27.
Previously, the white gene was mapped near anonymous EST markers on linkage group 3 of the Ambystoma meiotic map25.
The gene was mapped to chromosome 11 and was named cordon-bleu (cobl).
The bovine gene was mapped by somatic cell hybrid mapping panels to bovine chromosome BTA 25 with 94-95% concordance.
The Bph1 gene was mapped 3.8 cM from the STS marker BpE 18-3.
Eventually, the Bph6 gene was mapped onto rice chromosome 11 (Jena et al. 2002).
The gene was mapped to human chromosome 3q13.1-q13.2 by fluorescence in situ hybridization of cDNA probes to metaphase chromosomes.
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