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Some of the chemosensory gene family sizes in C. remanei may be overestimated since it has been demonstrated that genome sequences used for sequencing were extracted from heterozygotes [49].
For AhLOX7 and AhPLD, the unique sequences obtained from amplicon sequencing were extracted as references.
Strains for whole genome sequencing were extracted by using the DNeasy Blood and Tissue kit (QIAGEN).
A limited number of reference samples used for DNA sequencing were extracted by a method previously described by Kawasaki with minor modifications [ 8, 16].
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RNA used for hypoxia transcriptome sequencing was extracted from the whole brain.
gDNA for genome sequencing was extracted using two different methods.
Genomic DNA for genome sequencing was extracted exclusively from fresh young leaves after nuclear isolation.
Total RNA for RNA sequencing was extracted using the miRNEASY kit (Qiagen).
Codon 1, 2 and 1+2 sequences were extracted from CDS alignments and used as input for building trees, along with protein and CDS sequences.
Four sequences were extracted from GivenImaging capsule videos [4].
Candidate sequences were extracted from the 50 most highly upregulated genes from the microarray analyses.
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