Pair of primers for amplifying LINC02253 gene and application thereof
A primer pair and primer pair sequence technology, which is applied in the biological field, can solve the problems of unclear accuracy and specificity of the STC2 gene, and no diagnostic criteria are given, achieving good application prospects, saving time, and accurate results
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Embodiment 1
[0029] Specimen collection was approved by the Medical Ethics Committee of Nanjing Medical University.
[0030] Source of tissue samples: The samples came from 90 patients with colorectal cancer who were treated in the General Surgery Department of the First Affiliated Hospital of Nanjing Medical University between February 2015 and February 2016. (2) No radiotherapy, chemotherapy or other anti-tumor treatment before operation.
[0031] The collected information includes the patient's hospital number, name, gender, age, place of birth, contact address, telephone number, family history of cancer, colonoscopy results, important imaging examination data, surgical records, and postoperative pathological diagnosis results. If the initial record is incomplete, it will be supplemented and perfected later with the help of the hospital's electronic medical record system and the archived data in the medical record room. The relevant information that can be disclosed includes age, gende...
Embodiment 2
[0048] We further verified the expression level of the LINC02253 gene in 96 clinical samples obtained. The collection of samples was approved by the Medical Ethics Committee of Nanjing Medical University.
[0049] Source of tissue samples: The samples came from 90 patients with colorectal cancer who were treated in the General Surgery Department of the First Affiliated Hospital of Nanjing Medical University between February 2015 and February 2016. (2) No radiotherapy, chemotherapy or other anti-tumor treatment before operation. The collected information includes the patient's hospital number, name, gender, age, place of birth, contact address, telephone number, family history of cancer, colonoscopy results, important imaging examination data, surgical records, and postoperative pathological diagnosis results. If the initial record is incomplete, it will be supplemented and perfected later with the help of the hospital's electronic medical record system and the archived data in...
Embodiment 3
[0073] Example 3 LINC02253 expression level in TCGA database
[0074] TCGA (The Cancer Genome Atlas) was initiated by the U.S. government to try to map out the genome variation maps of all human cancers by applying genome analysis technology, especially large-scale genome sequencing, and conduct systematic analysis to find all cancer-causing genes. and small mutations of tumor suppressor genes, understand the occurrence and development mechanism of cancer cells, obtain new diagnosis and treatment methods on this basis, and finally outline the whole new "cancer prevention strategy". Jointly conducted by the National Cancer and Oncology Institute (NCI) and the National Human Genome Research Institute (NHGRI), it is expected to cost $100 million.
[0075]Use the Bioconductor / TCGAbiolinks function package to download and preprocess the mRNA expression RNASEqV2 data of the colorectal cancer dataset (COAD READ) from the TCGA database (http: / / tcga-data.nci.nih.gov / tcga / ), (643 tumors...
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