phred-polyphred software (CodonCode corporation)
90
Structured Review
CodonCode corporation
phred-polyphred software
Phred Polyphred Software, supplied by CodonCode corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/phred+software/phred+polyphred+software/pm19252810-36-5-7
Average 90 stars, based on 1 article reviews
Phred Polyphred Software, supplied by CodonCode corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/phred+software/phred+polyphred+software/pm19252810-36-5-7
Average 90 stars, based on 1 article reviews
phred-polyphred software - by Bioz Stars,
2026-10
90/100 stars
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Software:Article Title: Long-term follow-up of patients with recessive dystrophic epidermolysis bullosa in the Netherlands: expansion of the mutation database and unusual phenotype-genotype correlations. Article Snippet: Background: The current classification of recessive dystrophic epidermolysis bullosa (RDEB) comprises two major subtypes: ‘severe generalized RDEB’ (RDEB-sev gen) with early-onset, extensive, generalized blistering and scarring, complete absence of type VII collagen, and bi-allelic COL7A1 null mutations; milder ‘generalized other RDEB’ (RDEB-O) with reduced-to-normal type VII collagen expression, and Article Title: Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes. Article Snippet: Sequence data were analyzed using Sequencing:Article Title: Long-term follow-up of patients with recessive dystrophic epidermolysis bullosa in the Netherlands: expansion of the mutation database and unusual phenotype-genotype correlations. Article Snippet: Background: The current classification of recessive dystrophic epidermolysis bullosa (RDEB) comprises two major subtypes: ‘severe generalized RDEB’ (RDEB-sev gen) with early-onset, extensive, generalized blistering and scarring, complete absence of type VII collagen, and bi-allelic COL7A1 null mutations; milder ‘generalized other RDEB’ (RDEB-O) with reduced-to-normal type VII collagen expression, and Article Title: Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes. Article Snippet: Sequence data were analyzed using Mutagenesis:Article Title: Long-term follow-up of patients with recessive dystrophic epidermolysis bullosa in the Netherlands: expansion of the mutation database and unusual phenotype-genotype correlations. Article Snippet: Background: The current classification of recessive dystrophic epidermolysis bullosa (RDEB) comprises two major subtypes: ‘severe generalized RDEB’ (RDEB-sev gen) with early-onset, extensive, generalized blistering and scarring, complete absence of type VII collagen, and bi-allelic COL7A1 null mutations; milder ‘generalized other RDEB’ (RDEB-O) with reduced-to-normal type VII collagen expression, and Article Title: Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes. Article Snippet: Sequence data were analyzed using |