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A segment of 158,063 nucleotides of the pig major histocompatibility complex (SLA) and corresponding to the junction of the class I and class III regions was sequenced entirely using Sanger method.
1,763 reads of subclones ends were run on a LICOR 4200 sequencer and the sequences were assembled into contigs using Phred and Phrap software. Gaps between contigs were filled and sequenced by walking, and poor quality sequences were determined using 116 primers and dye terminators on an automated ABI 377 sequencer.
Contacts : Laurence Cattolico (Genoscope) - Patrick Chardon (INRA CEA)