The reference sequence (RefSeq) genome assembly is derived from the submitted GenBank assembly (see linked project PRJNA19967). Annotation provided on the RefSeq genomic records is based on NCBI annot
Our goal was to use ddRADseq to test for bias in SNP genotypes and genome coverage when using whole genome amplified DNA (via multiple displacement amplification) compared with raw genomic DNA.
Our goal was to use ddRADseq to test for bias in SNP genotypes and genome coverage when using whole genome amplified DNA (via multiple displacement amplification) compared with raw genomic DNA.
