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Geographic data were assembled as described elsewhere (Kidd et al., unpub. data).
Data were assembled as longitudinal survey panel data for analysis.
Data were assembled as monthly counts of all suicides and monthly counts of suicide separately for men and women.
The paired data were assembled as follows: 12 paired samples (six HN and six DCIS) were pulled from the data published by Emery et al. [ 15], two HN samples were pulled from the data published by Graham et al. [ 21], and the two matching pairs of DCIS samples (combined to equal 16 paired samples) were collected and processed from tissue acquired from the same patient.
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Histone octamers were assembled as follows [31].
TMA blocks were assembled as follows.
The 454-pyrosequencing data were assembled to serve as a reference sequence for future studies to identify gene duplications from allelic variations and to distinguish true/false SNPs.
Sequence data were assembled using NewBler assembler and Consed.
The GS FLX sequence data were assembled using Newbler assembly software.
PCR fragments were cloned, and sequenced using T7 and SP6 primers, and resulting sequence data were assembled into contigs using CAPs as described previously.
Sequence data were assembled into the complete genome sequence and analyzed as described elsewhere (2, 4 ).
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