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These mouse genes were mapped to human based on the Human and Mouse Orthology in the MGI database to obtain the orthologous human genes.
The gene was mapped to human chromosome 4q26 q27.
The gene had four exons separated by three introns and was mapped to human chromosome 12q13.
In 1990, my group published evidence that the gene we named BRCA1 mapped to human chromosome 17.
Reads were first mapped to human miRNA precursors, with unmapped reads used in the next step to map to snoRNAs.
Quality-filtered reads were then mapped to human genome (hg19) using STAR, and only the uniquely mapped reads were kept.
Blood meal reads primarily mapped to human genes, with a small number also showing homology with rat/mouse and dog genes.
Reads were mapped to Human GRCh38 (GCA_000001405.15) with dbSNP150 and Ensembl 90 annotation using HISAT249, and annotated against dbSNP150 and Ensembl 90.
ChIP-seq data were mapped to human genome (GRCh37/hg19) by using Bowtie2 and the HOMER software and ngsplot 2.47 were used to count normalized reads to generate box-plots and tag density plots, respectively.
The gene is highly conserved in evolution and has been mapped to human chromosome 21.
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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