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Figure 1 | BMC Genomics

Figure 1

From: Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region

Figure 1

Sequenced BAC contig and transcriptional map of chromosome 15q11-q13. (A) Genomic super-contig. Four contigs are diagramed and four gaps are shown with no data shown centromeric to BP1. The exact sizes of the gaps are currently unknown. (B). The order of genes in the PWS candidate region displayed in UCSC, Ensembl, and NCBI human genome browsers. # indicates that WHDC1LI is only displayed in the UCSC browser but not in the Ensembl and NCBI browsers. (C) Detail of sequence-based BAC contig. Only one BAC representing each position is diagramed, and the scale is not proportional to genomic size. The size of each BAC was recorded from the current entry in Genbank and readers should refer to the database for the most recent information if necessary. Two sequence gaps are shown in the map as filled balck bars.

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BMC Genomics

ISSN: 1471-2164

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