Samsung Electronics Co., Ltd.

Snu Rdb Foundation

Tae-Jin Ahn

Kyung-hee Park

Yeon-Su Lee

Jae-Heup Kim

Yun-Sun Nam

Kyu-sang Lee

Seung-Hak Choi

Su-hyeon Kim

Rangavittal Narayanan

Kyu-Sang Lee

Ok-ryul Song

Vishal Bhola

Shyamsunder Ajit Bopardikar

Byung-Chul Kim

Sung-young Lee

Min-Sun Kim

Kyoung-Gu Woo

SoYeon Ahn

Ji-young Oh

Taesung Park

Jung-nam Lee

Kyusang Lee

Nam Hwi Hur

Jong-suk Chung

Jong-Hoon Park

Jung-joo Hwang

Yeon-a Park

Ok-kyoung Son

Ki-Eun Kim

Ji-Young Cho

Moon-Soo Lee

Yun-sun Nam

Hyo-jeong Jeon

Dae-Soon Son

Iqbal Nadir Cazi

Rama Srikanth Mallavarapu

Jong-Suk Chung

Jhin-gook Kim

Jung-Nam Lee

Sung-ho Won

Seung-yeoun Lee

Bora Yeon

Young-ho Park

Jung-Hwan Song

Seung-Hak 403-1004 Kachi Maeul Sunkyung Apt Choi

Jung-Joo 206-1504 Dongsuwon Hwang

Yeon-Su 1003-102 Seongjeo Maeul Kunyoung Lee

Ji-Young Oh

Yeon-Su 1003-102 Seongjeo Maeul 13-Danji Lee

Ok-Kyoung Son

Ok-Ryul Song

Hyo-Jeong Jeon

Kyung-Hee Park

Yeon-A Park

A method of compressing sequence data in a text-based format, the method involving parsing text of the sequence data into a plurality of fields, identifying encoding algorithms that achieve greatest compression gains with respect to the plurality of fields based on collected statistics, and generating a bitstream, compressed from the sequence data, by encoding the sequence data using the identified encoding algorithms.

Method and apparatus for compressing genetic data

Provided are methods and apparatuses for compressing genetic information, the methods and apparatuses obtaining read information about reads and alignment information about positions of the reads that are aligned to a reference sequence, and generating a compressed file comprising information about an address of a block corresponding to the aligned reads. Also, a method and apparatus for decompressing genetic information obtains a compressed file with respect to the genetic information, determines an address of a block corresponding to input gene search information, from the compressed file, and selectively decompresses genetic information corresponding to the determined address.

Method and apparatus for compressing and decompressing genetic information obtained by using next generation sequencing (NGS)

An efficient and accurate method of identifying a target biomolecule in a sample by using target molecule-probe binding frequencies is disclosed.

Method of identifying target biomolecule by using probe-binding frequency

A method of recovering a nucleic acid sequence using a probe map includes: aligning a probe onto a target sequence based on a result in which the probe is hybridized to the target sequence; determining a representative value representing each aligned position of the probe; and recovering a base sequence of the target sequence by using a probe map to which the determined representative values and base sequence information of the probe are mapped.

Method and apparatus for recovering gene sequence using probe map

A method and apparatus for searching compressed nucleic acid sequences are disclosed. In the method, a reference sequence is compared with a subject sequence to be encoded, the subject sequence is compressed, an index is created with respect to the reference sequence and the compressed subject sequence, a position corresponding to a query is searched for in the compressed subject sequence using the index, a character found at the position within the compressed sequence is converted into a sequence, and the sequence is output as the response to the query.

Method and apparatus for searching nucleic acid sequence

A method and apparatus for monitoring a code to detect intrusion code is used to monitor target code to determine whether the target code is a resident code in a system or an intrusion code into the system. A first code pattern is extracted from the target code and a second code pattern is loaded from a storage unit, and a distance between the first code pattern and the second code pattern is calculated. The calculated distance is compared to a threshold to determine whether the target code is an intrusion code.

Method of and apparatus for monitoring code to detect intrusion code

Provided is a multiple single nucleotide polymorphism (SNP) for colorectal cancer diagnosis, a microarray and a kit including a polynucleotide having the SNP, and a method of diagnosing colorectal cancer using the SNP. Early diagnosis of incidence or possibility of colorectal cancer can be effectively performed by using the method.

Multiple SNP for diagnosing colorectal cancer, microarray and kit comprising the same, and method of diagnosing colorectal cancer using the same

A method of designing probes for detecting a target sequence and a method of detecting the target sequence using the probes are provided. The method of designing probes for detecting target sequence includes: selecting an anchoring location in the target sequence; selecting a first probe designing region; selecting a matched probe; and selecting a mismatched probe.

Method of designing probes for detecting target sequence and method of detecting target sequence using the probes

Provided is a polynucleotide for diagnosis or treatment of breast cancer, including at least 10 contiguous nucleotides of a nucleotide sequence selected from the group consisting of nucleotide sequences of SEQ ID No: 1 to SEQ ID No: 5 and comprising a nucleotide at 101position of the nucleotide sequence, or a complementary polynucleotide thereof.

Polynucleotide associated with breast cancer comprising single nucleotide polymorphism, microarray and diagnostic kit comprising the same and method for diagnosing breast cancer using the same

Provided are methods of storing, aligning, and retrieving haplotype data. A method of storing the haplotype data includes: determining the order of alleles in each single nucleotide polymorphism position of the haplotype data; aligning the haplotype data according to the order; and storing the aligned haplotype data in a predetermined data structure.

Methods of storing, aligning, and retrieving haplotype data

A multiple single nucleotide polymorphism (multi-SNP) marker for cardiovascular disease diagnosis and a method of diagnosing cardiovascular disease are provided. Also, sets of polynucleotides, a microarray, and a kit including the microarray are provided.

Multiple SNP for diagnosing cardiovascular disease, microarray and kit comprising the same, and method of diagnosing cardiovascular disease using the same

An isolated protein having an amino acid sequence of SEQ ID No. 4 and having an activity inducing apoptosis, and a gene encoding the same are provided. Also, a microarray having a substrate on which the gene or fragment thereof is immobilized is provided. Also, a method of diagnosing breast cancer using an antibody specifically binding to the protein and a method of diagnosing breast cancer by determining whether the gene is expressed in a cell or not, are provided.

Breast cancer related protein, gene encoding the same, and method of diagnosing breast cancer using the protein and gene

Provided is a method of predicting risk of lung cancer recurrence in a lung cancer patient or after a patient has lung cancer treatment, the method including: obtaining a biological sample from a lung cancer patient; measuring an expression level of at least one marker gene from the biological sample, the marker gene being selected from the group consisting of marker genes of Table 1, 2 or 3, to obtain data for the expression level of the marker gene; and determining whether the expression level of the marker gene corresponds to an expression level of a recurrence group or an expression level of a non-recurrence group.

Method of predicting risk of lung cancer recurrence, and a composition, kit and microarray for the same

A method of diagnosing breast cancer in an individual aged younger than 41 or older than 54 is provided. The method comprises obtaining a nucleic acid from the individual and determining a nucleotide at a polymorphic site of the nucleic acid. Polynucleotides specific to breast cancer, a microarray comprising the polynucleotides, and diagnostic kits are also provided.

Method of diagnosing breast cancer and compositions therefor

There is provided a method of designing a probe from a polynucleotide group comprising a plurality of polynucleotides, the method including: forming a polynucleotide group by selecting polynucleotides having a certain sequence; producing polynucleotide fragments having a certain length from each of the polynucleotides of the polynucleotide group and obtaining sequence and position information on the polynucleotide fragments; providing each polynucleotide fragment with a sequence specific identification number using the obtained sequence and position information of the polynucleotide fragments; and comparing the identification numbers of the fragments to select the probe.

Method of designing probe from polynucleotide group comprising plurality of polynucleotides

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Seoul, South Korea

Tae-Jin Ahn