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The porB sequences exhibited length polymorphism.
The two sequences exhibit 78.8% sequence identity.
No genes in the 383,367-bp sequence exhibited homology to mitochondrial aldehyde dehydrogenase, glycine-rich protein, or retrograde regulated male sterility protein, which were encoded by maize Rf2a, rice Rf2, or rice Rf17, respectively (Table 1).
Subfamily 1 consists of rice, wheat, switchgrass, sorghum, and maize sequences.
Silico3 was predicted from the B73 maize sequences.
Maize sequences for design of this chip were predominantly selected from the The Institute for Genomic Research TIGRR) maize gene index [ 33].
The scanned maize sequences represent the whole large sequences available for maize in the public database, i.e., excluding the trace files and the gene-only sequences.
Maize sequences were identified by local BLASTP program as described above.
Transcripts with best matches to viral or maize sequences were removed from further analyses.
The maize biochar exhibited stronger structural surface functional groups including aromatic CC stretching.
The public maize sequence sets fall into three classes: (A) maize whole genome sequences, (B) maize repeats, and (c) maize gene enrichment sequences.
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