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Based on the land use change, Pre-European genosoils and present genosoils and phenosoils were identified and mapped within each of the Pre-European soil classes.
We divided the entire genome into 100 kb segments and counted the number of reads mapped within each segment.
To determine RNA transcriptional abundance for each gene, the number of reads that mapped within each annotated coding sequence (CDS) was determined.
The number of reads mapped within each annotated transcript was calculated in order to estimate the level of transcription for each gene.
To estimate the level of transcription for each gene, the number of reads that mapped within each annotated coding sequence (CDS) was determined.
Community assets including religious congregations, key and support food pantries, and public parks were identified and mapped within each of the neighborhoods around the four intervention schools.
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The mapped DNA sequences were concatenated if more than two reads were mapped within 90 nt of each other.
The approach we took in the past when looking for duplicate alleles among mapped emb mutants was to limit complementation tests to mutants disrupted in genes that mapped within 5 cM of each other [9].
Using a Landsat time-series, the age of first clear-cutting that could be mapped within the boundaries of each property had a negative effect on the proportion of upland, riparian, and total forest cover retained.
We included markers that mapped within 10 kb of each candidate gene according to NCBI36/hg18.
For this calculation, we used only reads that mapped within 1,000 bp of each other when aligned to the reference.
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