109 results about "Chromosome number" patented technology

The invention discloses a method and a device for quick contrast and analysis of a short sequence for second-generation sequencing, which can solve the problems of low contrast efficiency and high memory occupation ratio of sequencing data. The method comprises the following steps of obtaining a DNA (deoxyribonucleic acid) short sequence obtained by sequencing, and respectively mapping and encoding the DNA short sequence by a first hash algorithm and a second hash algorithm, so as to respectively obtain a first index and a second index; according to a preset index query library, the first index and the second index, contrasting the DNA short sequence and a reference gene group, wherein the index query library consists of an unit structure array, and each unit structure comprises value and index 2; storing the array index offset of each unit structure as the corresponding index 1, namely the index value corresponding to the structure array, wherein K is the length of segment sequence; according to the contrast result, when the contrast result is correct, obtaining the value of the K-mer segment contrasted with the corresponding DNA short sequence, and determining the chromosome number of the corresponding DNA short sequence and the site on the chromosome.

The invention discloses a gene analysis annotation method and device. The method comprises the following steps that: capturing first gene data from at least one existing gene database; storing the first gene data in a uniform format, and constructing an annotation gene database; obtaining a standard file used for describing genome variation, and extracting a retrieval value from the standard file; according to the retrieval value, carrying out retrieval in the annotation gene database to obtain second gene data, wherein the retrieval value comprises the chromosome number of a variation site, the starting position of the variation site, the basic group of a refereed genome and the basic group of the variation site; and according to the second gene data, carrying out gene annotation on the standard file, and generating a gene analysis annotation result report. By use of the method, the gene analysis annotation can be accurately and efficiently carried out.

The invention discloses technology for culturing a unisexual hybrid scallop by utilizing a purple scallop and a bay scallop, which relates to shellfish breeding technology for aquiculture. The technology comprises the steps of: utilizing two congeneric hermaphroditic scallops with same chromosome number; ripening the two scallops respectively to achieve the synchronous maturity; and then synchronously inducing the two scallops to spawn and spermiate; and acquiring sperms and ovum of the two scallops respectively for interspecies cross-insemination to culture the unisexual hybrid scallop. Obtained offsprings have separated sexes, have males and females, and also have hermaphroditic individuals; ovum from female individuals in the hybrid offsprings can be inseminated by any parental sperm and normally grow; and the hermaphroditic individuals in the hybrid offsprings can be used for quickly purifying a strain.

The invention relates to an approach of searching gene group sequence database based on characters. Approximate sequence is searched in database according to sequence statistic character. The search method is as follows: search approximate sequence according to distance of statistic character, namely, basic information of different species' sequence group serial data, including sequence's database login number, species name, chromosome number, original data, basic group composition character and base pair relativity character is memorized in database. For any a gene snippet submitted by client, its eigenvalue is computed according to client's request and distance between the eigenvalue and all corresponding eigenvalue in database is computed to compare approximate sequence; the most approximate sequence is arranged and displayed by distance.

The invention provides an automatic separation method for conglutinated chromosomes. The method firstly carries out immersion and corrosion processing operation based on a grey scale characteristic graph of chromosomes, and then carries out conditioned expansion recovery processing operation. The invention designs a grey scale characteristic graph-based morphological processing method to separate the chromosomes which are seriously conglutinated but are neither sheltered nor overlapped. The method solves the technical problems and fills up the technical vacancy of separating the chromosomes which are seriously conglutinated but are neither sheltered nor overlapped in the prior art, meets the requirements of accurately separating the conglutinated chromosomes and detecting the number of the chromosomes in medical fields of chromosome analysis, cell research, pathological analysis, and the like, and further improves the automaticity in a chromosome analysis system. The method provides individual chromosomes with good continuous boundary effect and independence for the automatic separation processing in the chromosome analysis system, and particularly keeps concave and convex details of original chromosome image boundary completely and clearly so as to improve the separation automaticity of the conglutinated chromosomes and the accuracy of the chromosome number counting.

The invention discloses a seedless grosvenor momordica with high mogroside content, high whole fruit utilization rate and good taste, and a cultivating method for the seedless grosvenor momordica. The steps of the method are as follows: 1) cultivating and planting the diploid female and male seedlings of the grosvenor momordica; 2) when a male plant emerges a flower bud, inducing the formation of diploid big pollen; 3) picking the male flower that is induced to bloom and screen a diploid big pollen therein; 4) hybridizing the haploid oocyte of the diploid female plant after treating the diploid big pollen in the pollen germination solution, acquire the hybrid seeds after the female plant fruits; 5) propagating the hybrid seed into whole plant and then screening a triploid plant with the Chromosome number inspection; 6) planting the triploid plant and the diploid male plant, and carrying out artificial pollination to the male triploid plant with the male diploid plant when the plant is blooming, thus acquiring the seedless grosvenor momordica when the female plant fruits.

A method for detecting the number of human chromosomes NO.21 by real-time quantitative PCR technique in order to diagnoise the triple-21 syndrome includes such steps as using the genome-specific single-cope sequence as the molecular marker of chromosome, choosing part of non-polymorphic fragments of DSCR4 gene as target molecular marker, choosing part of fragments of RABIF gene as internal reference molecular marker, designing two pairs of primers and relative Taqman probes, amplifying said two sequences in a single tube by PCR, determining the relative value deltact, and determining the number of chromosomes No.21.

Methods for producing hybrids between domestic and wild soybean that are fertile and can be further bred with other soybean plants are provided, thus allowing transfer of desirable traits and genes from the wild soybean into the domestic soybean. This invention also provides novel media for producing callus and multiple somatic embryos, as well as novel media for producing multiple shoots from the embryos. The hybrid plants are made fertile by colchicine treatment to double their chromosome number so that they can be backcrossed into domestic soybean. These methods and media allow the production of elite soybean lines containing traits or genes from wild soybean as well as a minimum amount of additional wild soybean DNA. Backcrosses containing only one wild soybean chromosome can be produced, as well as sets of such backcrossed lines that each contain one chromosome from the wild ancestor, but collectively all the wild chromosomes from the hybrid ancestor. Plants and plant progeny and plant tissue (tissue including seeds) of plants produced by the foregoing methods are also provided. The methods do not require genetic modification, and thus this invention allows production of domestic soybean plants that are not genetically-modified organisms (non-GMO) but that express desirable traits derived from wild soybean.

The invention discloses a cultivating and planting method of a begonia named Yinjiao. According to the invention, an artificial pollination method is adopted, begonia dryadis irmsch. is adopted as a female parent, B.'White King' is adopted as a male parent, and sexual hybridization is carried out; an offspring individual plant is subject to self-pollination, and the variety Yinjiao is obtained through selective breeding from an F2 generation colony; the chromosome numbers of the parents and the filial generation are determined; and the variety Yinjiao obtained through the previous cultivationsteps is planted in humic soil under a temperature of 15-25 DEG C and an air relative humidity of 65-75%, where in the humic soil is air-permeating and is rich in organic matters. Also, the drainage of the humic soil is good.

The invention discloses a method for cultivating a corn allopolyploid by using an unreduced gamete characteristic of tripsacum dactyloides, belonging to the field of corn distance hybridization. The method comprises the steps of: hybridizing an MTF-1 (metal-responsive transcription factor) as a female parent with corn or tetraploid perennation corn as a male parent, and then selecting a filial generation plant which is capable of overwintering, namely a new corn allopolyploid, wherein the tiller number of the filial generation plant is more than 15 and the chromosome number of the filial generation plant is a sum of the chromosome number of a female parent and the chromosome number of the male parent. According to the method provided by the invention, the dysgenesis of corn affinis species is overcome and a good inheritance basis is provided for breeding ground-breaking corn species by using the bred corn allopolyploid as a bridge material transfer character. In addition, the method provided by the invention provides a model to breed allopolyploids of other species. The corn allopolyploid bred by the method provided by the invention is perennial, adopts vegetative propagation, and provides a material to corn allopolyploid origin and evolution research and allopolyploid breeding. The method provided by the invention is simple, is short in time, high in efficiency and small in workload.

The invention relates to an industrial production method of Cymbidium germchit based on sexual hybridization. The method provided by the invention comprises the following steps of: firstly identifying chromosome number and ploidy of Cymbidium parents; selecting pairing hybridized combinations according to the ploidy; carrying out a sexual hybridization pollination of the Cymbidium; managing the pollinated Cymbidium; carrying out a nonsymbiotic germination culture on Cymbidium seeds; inducing and differentiating protocorms (PLBs) of the Cymbidium seeds; differentiating bigger seedlings of the Cymbidium; transplanting the Cymbidium seedlings into bottles; and managing the cultivation of the Cymbidium transplanted seedlings. On the basis of indentifying the chromosomes of the Cymbidium parents, the method provided by the invention selectively pairs the hybridized combinations and carries out the sexual hybridization pollination, so that the aims of improving varieties and breeding new varieties are achieved; then a lot of Cymbidium germchit can be industrially produced through a tissue culture method.

The invention relates to a method for producing haploid plant embryos, comprising providing microspores or pollen that comprise cell division inducing molecules; pollinating an embryo sac cell, in particular an egg cell, of the plant of which the haploid embryo is to be made with the microspores or pollen; allowing the microspores or pollen to discharge the cell division inducing molecules in or in the vicinity of the embryo sac cell, in particular the egg cell, to trigger division thereof to obtain a haploid plant embryo. When doubled haploid plant embryos are to be produced doubling of the chromosome number takes place at a certain stage after pollination, in particular during cell division or after obtaining the embryo. The invention further relates to the embryos thus obtained, plants regenerated therefrom and progeny thereof.

The invention discloses two polyploid centella asiatica varieties and a cultivation method thereof. The cultivation method comprises the following steps of 1, selecting terminal buds of a diploid centella asiatica adult plant, and carrying out breeding of a tissue cultured seedling or callus tissue, 2, carrying out chromosome doubling induction culture and differentiation culture of tissue subcultured seedling or callus tissue by oryzalin, 3, cutting down novel buds obtained by the differentiation culture and carrying out cluster bud culture, 4, carrying out chromosome doubling identification of the cultured complete plants having roots, stems and leaves, screening the tetraploid plant, and planting the tetraploid plant to obtain the tetraploid centella asiatica variety, 5, carrying out artificial emasculation and pollination hybridization of the tetraploid plant and the diploid plant to obtain hybrid seeds (female parent 4N*male parent 2N or male parent 4N* female parent 2N, wherein F1 is 3x), and 6, breeding the hybrid seeds into complete plants, planting the plants, carrying out chromosome number detection and screening the triploid centella asiatica variety.

Wherein, with adult sperm cell of Maladera sp. As material, pre-processing for 6-14h with colchicine; using 0.4%KCl to hypotonic reaction for 30min; curing with methaol and glacial acetic acid (3:1) for 30-60min; finally, dyeing with Giemsa for 10-20min. this invention obtains clear chromosome with number as n = 9.

The invention provides a kit for detecting genotype of human chromosome 21 STR (short tandem repeat). The kit comprises an amplification reagent and an amplification product detection reagent and mainly contains primers of 12 pairs of fluorescent markers, a molecular weight internal label containing the size of 14 fragments, an allele typing standard product and a quality control product. According to the kit disclosed by the invention, when the kit is used, the required quantity of specimens is small, the diagnosis is fast, and the kit is suitable for villi, amniotic fluid, blood and other tissues, and can be used for not only prenatal diagnosis, but also source analysis of extra chromosomes of a 21-trisomy aborted fetus; the kit can precisely diagnose the genotype and is conductive to presentation of diagnosis result and laboratory quality evaluation; and the kit can further realize fast, accurate, automatic and high-throughput detection of the number of chromosomes 21 and realize quality controllability and standardization of a detection result, and thus has clinical application prospects.

The invention provides a method for identifying carnation chromosome number by bud, comprising: obtaining bud anther, ovary wall and corolla tissue, pre-treating ice water mixture, fixing by stationary liquid, dyeing, dissociating with hydrochloric acid, tabletting and microscopic examining. Compared with the traditional method that a root tip tissue is used for chromosome tabletting, the invention solves the disadvantages of few visual filed cells, difficult microscopic examination and poor chromosome dispersion during root tip chromosome tabletting, and overcomes the problems of long rootage period for carnation cutting seedling and time and labor wasting for cutting; compared with stem tip chromosome tabletting, the invention overcomes the interference problem of non-meristematic cell or reserve substance or secretion, chromosome tabletting can be realized only by using buds, which does not damage plant growing state and has convenient material resource; in addition, a plurality of metaphase cells exist, so that the difficulties of small carnation chromosome, huge quantity and hard counting of the chromosome can be solved. Thus, when plants bloom, the effective method is that the bud is used for chromosome tabletting.

The invention relates to an artificial cultivation and seedling industrial production method of a dendrobium nobile polyploid compound, which comprises the following steps of: carrying out artificial pollination in a flowering period of common dendrobium nobile, inoculating harvested seeds in a 1/2MS liquid nutrient medium for nonsymbiotic germination cultivation, transferring protocorm of seeds in a proembryo stage into a 1/2MS liquid nutrient medium containing 0.01% of colchicin for mutagenesis cultivation, then transferring into 1/2MS solid nutrient medium for cultivation till seedlings ofdendrobium nobile are formed, carrying out flowering cultivation on tetraplont seedlings with chromosome numbers of 2n=76, taking tetraplont as a female parent and diploid as a male parent or taking diploid as a female parent and tetraplont as a male parent for hybridization to obtain the triploid; transferring triploid hybridized seeds in a formation early state into the 1/2MS liquid nutrient medium containing 0.01% of colchicin for carrying out artificial mutation hexaploid treatment for 150-180h, and then transferring into the 1/2MS solid nutrient medium till the seedlings are formed, selecting seedlings with chromosome numbers of 2n=114 as tetraplont dendrobium nobile for carrying out bottle seedling transplanting, and finally cultivating and managing according to a conventional method till flowering. The invention lays the foundation for the popularization of new varieties of the dendrobium nobile.

The invention discloses a slide preparation method for discriminating the chromosome number of Avena magna, Triticum aestivum or a filial generation of Avena magna and Triticum aestivum. The method comprises the following steps: pretreatment; fixation; enzymatic hydrolysis; acidolysis; post-hypotonic treatment; post-fixation; slide preparation; slide compression; etc. Through improvement of conventional methods, the slide preparation method provided by the invention can effectively discriminate the chromosome number of Avena magna, Triticum aestivum or the filial generation of Avena magna and Triticum aestivum. Experimental results show that a slide prepared by using the slide preparation method has a good number of cell division phases and good chromosome dispersion, and high repeatability and reliable results are obtained. Thus, a novel method is provided for discriminating the chromosome number of Avena magna, Triticum aestivum or the filial generation of Avena magna and Triticum aestivum, and technical support is provided for hybridization and seed selection of Avena magna and Triticum aestivum.

The invention discloses a wheat-tritileymus 3D (3Ns) alien substitution line cultivation method, comprising the following steps: (1) hybridizing tetraploid durum wheat and octaploid tritileymus, authenticating every generation, and screening single plants with chromosome number (2n=42) and tritileymus Ns genome chromosomes; and (2) bagging the screened single plants, conducting selfing, and breeding a wheat-tritileymus alien substitution line with two tritileymus Ns genome chromosomes at the F5 generation. Furthermore, the invention also discloses an identification method for the quality of a wheat seed, and the identification method comprises a fluorescence in situ hybridization (FISH) method and an EST-STS (Expressed Sequence Tag-Sequence Tagged Sites) tag identification method. A wheat-tritileymus 3D (3Ns) alien substitution line cultured by using the method disclosed by the invention is remarkably improved on the aspects of agronomic traits such as plant height, ear length, tiller number and the like.

The invention relates to a three-dimensional inducing method for inducing a spermatogonia stem cell to differentiate into a functional sperm cell in vitro, and belongs to the field of bioengineering. On the basis of acquiring the spermatogonia stem cell, a three-dimensional culture system is established through Matrigel, a key factor for inducing differentiation is added, the spermatogonia stem cell is induced to differentiate in vitro to obtain the sperm cell having a fertilization ability, the sperm cell obtained through induction is identified through an immunocytochemical method, the chromosome number of the sperm cell obtained through induction is detected through fluorescence in situ hybridization (FISH), and the fertilization ability and the viability of the sperm cell obtained through induction are detected through round spermatid injection (ROSI). The application provides an excellent model for the molecular mechanism of the human sperm, and in addition, a functional gamete is provided for an azoospermia patient, so that a male infertility patient can have a child of his own.