| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_13bbe0db2ee42363f3aba3f4bd69c0a4 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-118
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-106 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6869
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6886
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C40B50-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6806 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6869
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6806
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6886
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C40B50-06 |
| filingDate |
2022-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aaf4f28c1045ff59c905ef5d713d75c9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b74d649d0b17af07837a3d0d6c8bd0ad
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_56a449e946a8a7752fbd990a4940b27c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_156504e4d40c5a5cc1a12b7e0cd8834d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11d5fb5e78f7dddc4a0a43f1787b5997 |
| publicationDate |
2022-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
CN-114686589-A |
| titleOfInvention |
Composition, kit, and sequencing library construction method for BRCA whole-exon gene mutation detection |
| abstract |
The invention relates to the technical field of molecular diagnosis, in particular to a composition, a kit and a sequencing library construction method for BRCA whole exon gene mutation detection. The targeted region of the specific amplification primer pair in the composition of the present invention includes the entire coding region; ±20bp at the junction of exon and intron; 5UTR region: full length of exon 2 + intron 1 at least 20bp; 3UTR Region: at least 20bp after the stop codon; the union of the coding regions of all transcripts; the length of the amplicon obtained by amplification with human genomic DNA as a template is 120bp-200bp, which can target and capture small fragments of DNA templates, and is used in DNA template extracted from FFPE samples to improve template utilization. |
| priorityDate |
2022-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |