METHOD FOR IDENTIFYING WHETHER A DIPLOID POTATO IS SELF-COMPATIBLE

    公开(公告)号:US20240188520A1

    公开(公告)日:2024-06-13

    申请号:US18436876

    申请日:2024-02-08

    摘要: The present application relates to the technical field of genetic breeding, and provides a method for identifying whether a diploid potato is self-compatible. The method relates to identifying whether a StSCI gene in the diploid potato is transcribed and expressed. Also disclosed is a method for identifying whether a StSCI gene is expressed by using molecular marker, and a method of screening for the molecular marker, which includes: obtaining the genome sequence information of parental materials, screening for difference sites of the parental materials, screening for the molecular marker, and identifying whether the screened molecular marker are usable. As for the identification of the self-compatibility of a diploid potato by using the screened molecular marker, the identification workload is small, a lot of time is saved, and the identification result is not affected by the environment, and it is accurate and reliable.

    FRAGMENTOMICS IN URINE AND PLASMA
    4.
    发明公开

    公开(公告)号:US20240182982A1

    公开(公告)日:2024-06-06

    申请号:US18523606

    申请日:2023-11-29

    IPC分类号: C12Q1/6886 C12Q1/6858

    摘要: Fragmentomic features provide various properties of the sample (e.g., urine or plasma) and/or of a subject. Relative contributions or enrichment of clinically-relevant DNA (e.g., type(s) of transrenal and non-transrenal urinary cfDNA) are provided using fragmentomic features of urinary cell-free DNA. Such measurements could be used for reflecting the glomerular permeability and monitoring various diseases, e.g., kidney abnormality. The fragmentomic features can include a corrected urinary DNA concentration, size, end motifs of urinary DNA molecules, and cfDNA molecules from open chromatin regions (OCR) of one or more tissues. In addition, nuclease activities or other fragmentation processes of cfDNA are determined based on relative contributions concerning the different profiles of cfDNA cleavage, which are also used for determining contribution of cfDNA from tissue(s), level of pathology, and gestational age.

    DUAL-PROBE METHOD FOR FLUORESCENCE QUANTITATIVE PCR

    公开(公告)号:US20240158844A1

    公开(公告)日:2024-05-16

    申请号:US18179192

    申请日:2023-03-06

    IPC分类号: C12Q1/6858 C12Q1/6818

    摘要: A dual-probe method for fluorescence quantitative PCR (Polymerase Chain Reaction) is disclosed. The method involves the use of a Taqman dual-probe detection system with the same pair of primers. The dual probes includes a detection probe and a reference probe. The detection probe targets the wild-type sequence at the hotspot mutation site, which can cover multiple adjacent mutations. The reference probe targets the wild-type sequence adjacent to the target sequence. Both probes share the same pair of upstream and downstream primers. This method uses a single reaction qPCR (quantitative PCR) method, which can simultaneously detect multiple adjacent mutations. It effectively saves tissue samples and greatly shortens the testing period. Moreover, the close proximity of the target and reference sequences enhances the reliability and accuracy of the results, making it widely applicable in various fields.