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AlleleID® |
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MLPA® Probe Design
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Probe Design: You can design MLPA® probes, both for
copy number detection and SNP studies. The software was
developed in collaboration with MRC
Holland, the inventors of the technology, and follows
all MLPA design guidelines. AlleleID® can also design
custom oligos for Pam4U PamChip® Arrays.
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Avoid Homology: AlleleID®
designs highly specific MLPA®probes by automatically
avoiding the regions of homology identified during a BLAST
search.
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Multiplex MLPA® Probes: Displays the free energies
of the most stable cross-dimers formed between the MLPA®
probes, helping you determine which probes are best suited
for a multiplex reaction.
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Load SNPs: Easily loads sequences containing SNPs from
the variation descriptors in standard GenBank variation
files and from UCSC file. If you are working with unpublished
data you can easily add them.
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Load Exons: Retrieves exon information from GenBank header
annotations and UCSC genome browser. If you are working
with unpublished data you can easily add them.
- Sequence View: AlleleID®
displays the designed MLPA® probes and where they bind
to the sequence.
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