標(biāo)題: Titlebook: Bioinformatics Research and Applications; 16th International S Zhipeng Cai,Ion Mandoiu,Xuan Guo Conference proceedings 2020 Springer Nature [打印本頁(yè)] 作者: 戰(zhàn)神 時(shí)間: 2025-3-21 19:13
書(shū)目名稱Bioinformatics Research and Applications影響因子(影響力)
書(shū)目名稱Bioinformatics Research and Applications影響因子(影響力)學(xué)科排名
書(shū)目名稱Bioinformatics Research and Applications網(wǎng)絡(luò)公開(kāi)度
書(shū)目名稱Bioinformatics Research and Applications網(wǎng)絡(luò)公開(kāi)度學(xué)科排名
書(shū)目名稱Bioinformatics Research and Applications被引頻次
書(shū)目名稱Bioinformatics Research and Applications被引頻次學(xué)科排名
書(shū)目名稱Bioinformatics Research and Applications年度引用
書(shū)目名稱Bioinformatics Research and Applications年度引用學(xué)科排名
書(shū)目名稱Bioinformatics Research and Applications讀者反饋
書(shū)目名稱Bioinformatics Research and Applications讀者反饋學(xué)科排名
作者: Derogate 時(shí)間: 2025-3-21 23:15
https://doi.org/10.1007/978-3-322-93111-5ion term to dispatch gene-disease associations to individual isoforms, and reversely aggregate these dispatched associations to affiliated genes. Next, it fuses different genomics and transcriptomics data to replenish gene-disease associations and to induce a linear classifier for predicting isoform作者: concert 時(shí)間: 2025-3-22 04:05
Funktionen und ihre Ableitungen,a and reduce the chance of filtering out potential candidates overlooked by a single clustering. In the search stage, EpIntMC applies Entropy score to screen SNPs in each cluster, and uses Jaccard similarity to merge the most similar clusters into candidate sets. After that, EpIntMC uses exhaustive 作者: surrogate 時(shí)間: 2025-3-22 05:04 作者: 催眠藥 時(shí)間: 2025-3-22 09:37 作者: 連系 時(shí)間: 2025-3-22 13:02
Konventionen und Begriffe zu diesem Buch,oth naturally occurring human variants and somatic mutations in cancer. In the context of cancer,?~3?M somatic mutations were extracted from over 10,000 cancerous human samples. Of the entire human proteome, 593 protein-coding genes show statistically significant bias towards harmful mutations. Thes作者: Emg827 時(shí)間: 2025-3-22 17:32
Konventionen und Begriffe zu diesem Buch,e classic structural variants that can be detected by state-of-the-art methods (e.g., SVIM and Sniffles), our experiments demonstrate recall improvements of up-to . without harming the precisions (i.e., above .). We also point out three directions to further improve structural variant detection in t作者: 發(fā)炎 時(shí)間: 2025-3-22 23:41 作者: 痛打 時(shí)間: 2025-3-23 03:01 作者: 吸引力 時(shí)間: 2025-3-23 07:30 作者: 容易生皺紋 時(shí)間: 2025-3-23 11:46 作者: 珠寶 時(shí)間: 2025-3-23 16:52 作者: Climate 時(shí)間: 2025-3-23 19:43
Isoform-Disease Association Prediction by Data Fusion,ion term to dispatch gene-disease associations to individual isoforms, and reversely aggregate these dispatched associations to affiliated genes. Next, it fuses different genomics and transcriptomics data to replenish gene-disease associations and to induce a linear classifier for predicting isoform作者: 賞心悅目 時(shí)間: 2025-3-24 01:09
EpIntMC: Detecting Epistatic Interactions Using Multiple Clusterings,a and reduce the chance of filtering out potential candidates overlooked by a single clustering. In the search stage, EpIntMC applies Entropy score to screen SNPs in each cluster, and uses Jaccard similarity to merge the most similar clusters into candidate sets. After that, EpIntMC uses exhaustive 作者: MARS 時(shí)間: 2025-3-24 04:52 作者: 卵石 時(shí)間: 2025-3-24 10:01
Ess-NEXG: Predict Essential Proteins by Constructing a Weighted Protein Interaction Network Based ontial proteins. In Ess-NEXG, we construct a reliable weighted network by using these data. Then we use the node2vec technique to capture the topological features of proteins in the constructed weighted PPI network. Last, the extracted features of proteins are put into a machine learning classifier t作者: Bone-Scan 時(shí)間: 2025-3-24 12:14 作者: 過(guò)濾 時(shí)間: 2025-3-24 18:19
SVLR: Genome Structure Variant Detection Using Long Read Sequencing Data,e classic structural variants that can be detected by state-of-the-art methods (e.g., SVIM and Sniffles), our experiments demonstrate recall improvements of up-to . without harming the precisions (i.e., above .). We also point out three directions to further improve structural variant detection in t作者: 錯(cuò) 時(shí)間: 2025-3-24 20:51
Prediction of Drug-Target Interaction via Laplacian Regularized Schatten-p Norm Minimization,ew drug/target cases by combining the loss function with a Laplacian regularization term. Finally, we numerically solve the LRSpNM model by an efficient alternating direction method of multipliers (ADMM) algorithm. Performance evaluations on benchmark datasets show that LRSpNM achieves better and mo作者: 亞當(dāng)心理陰影 時(shí)間: 2025-3-25 00:13 作者: pulse-pressure 時(shí)間: 2025-3-25 04:09 作者: nullify 時(shí)間: 2025-3-25 09:17 作者: Conflict 時(shí)間: 2025-3-25 11:58
0302-9743 ions. They were organized in topical sections named: genome analysis; systems biology; computational proteomics; machine and deep learning; and data analysis and methodology..978-3-030-57820-6978-3-030-57821-3Series ISSN 0302-9743 Series E-ISSN 1611-3349 作者: Admonish 時(shí)間: 2025-3-25 16:19 作者: indecipherable 時(shí)間: 2025-3-25 22:57 作者: conjunctiva 時(shí)間: 2025-3-26 01:25
Der alte Mensch im Krankenhaus,library with novel discriminative k-mers from the input sequencing reads. We evaluated the performance in different conditions against several other tools and the results showed an improved F-measure, especially when close reference genomes are not available..Availability: 作者: 討人喜歡 時(shí)間: 2025-3-26 06:19
https://doi.org/10.1007/978-3-662-58792-83% and . of letters on reads to identical letters on reference genomes for human individuals of Nanopore and SMRT data sets, respectively. The state-of-the-art method can only align . and . letters of reads for Nanopore and SMRT data sets, respectively. Our method is also faster than the state-of-the-art method....作者: 溝通 時(shí)間: 2025-3-26 11:39
,Komplikationen der Durchblutungsst?rung, criterion of hotspot selection for all cancer types but there are three to four distinct groups of cancer with similar properties. Overall the presented results point to the necessity to choose different hotspots selection criteria for different types of cancer.作者: 戰(zhàn)勝 時(shí)間: 2025-3-26 13:07 作者: hyperuricemia 時(shí)間: 2025-3-26 17:01
Identification of a Novel Compound Heterozygous Variant in , Causing Bone Fragility by the Type of sidues and predicted to be highly damaging. Timely health care of patients with such a set of clinical spectrum of SOPH syndrome, ALF and bone fragility by the type of OI can contribute to establishment coordinated multispecialty management of the patient focusing on the health problems issues through childhood.作者: 投票 時(shí)間: 2025-3-26 23:37
Improving Metagenomic Classification Using Discriminative k-mers from Sequencing Data,library with novel discriminative k-mers from the input sequencing reads. We evaluated the performance in different conditions against several other tools and the results showed an improved F-measure, especially when close reference genomes are not available..Availability: 作者: 神經(jīng) 時(shí)間: 2025-3-27 04:39 作者: 路標(biāo) 時(shí)間: 2025-3-27 07:27
Cancer Breakpoint Hotspots Versus Individual Breakpoints Prediction by Machine Learning Models, criterion of hotspot selection for all cancer types but there are three to four distinct groups of cancer with similar properties. Overall the presented results point to the necessity to choose different hotspots selection criteria for different types of cancer.作者: Dna262 時(shí)間: 2025-3-27 12:42
Conference proceedings 2020ssia, in December 2020.. The 23 full papers and 18 short papers presented in this book were carefully reviewed and selected from 131 submissions. They were organized in topical sections named: genome analysis; systems biology; computational proteomics; machine and deep learning; and data analysis an作者: Infuriate 時(shí)間: 2025-3-27 13:50
Warenbuchungen (ohne Umsatzsteuer), (2) devise an exact algorithm for decisiveness, (3) develop problem reduction rules, and use them to obtain efficient algorithms for inputs with few loci, and (4) devise an integer linear programming formulation of the decisiveness problem, which allows us to analyze data sets that arise in practice.作者: 遭受 時(shí)間: 2025-3-27 18:12
Checking Phylogenetic Decisiveness in Theory and in Practice, (2) devise an exact algorithm for decisiveness, (3) develop problem reduction rules, and use them to obtain efficient algorithms for inputs with few loci, and (4) devise an integer linear programming formulation of the decisiveness problem, which allows us to analyze data sets that arise in practice.作者: medieval 時(shí)間: 2025-3-27 21:57
0302-9743 Moscow, Russia, in December 2020.. The 23 full papers and 18 short papers presented in this book were carefully reviewed and selected from 131 submissions. They were organized in topical sections named: genome analysis; systems biology; computational proteomics; machine and deep learning; and data a作者: incite 時(shí)間: 2025-3-28 05:09
https://doi.org/10.1007/978-3-8351-9029-0mutations collected in public databases such as PhyloTree. Experimental results on real and simulated datasets show that our mutation analysis methods have accuracy comparable to that of state-of-the-art methods based on haplogroup frequency estimation for both single-individual samples and two-individual mixtures, with a much lower running time.作者: 拋物線 時(shí)間: 2025-3-28 06:35 作者: 我吃花盤(pán)旋 時(shí)間: 2025-3-28 13:35 作者: 使人入神 時(shí)間: 2025-3-28 16:10 作者: 描述 時(shí)間: 2025-3-28 22:27
Conference proceedings 2020ssia, in December 2020.. The 23 full papers and 18 short papers presented in this book were carefully reviewed and selected from 131 submissions. They were organized in topical sections named: genome analysis; systems biology; computational proteomics; machine and deep learning; and data analysis and methodology..作者: 索賠 時(shí)間: 2025-3-29 00:23
Lecture Notes in Computer Sciencehttp://image.papertrans.cn/b/image/187172.jpg作者: 價(jià)值在貶值 時(shí)間: 2025-3-29 03:41
https://doi.org/10.1007/978-3-8351-9029-0duced efficient inference algorithms based on Jaccard similarity between variants called from high-throughput sequencing data of such DNA samples and mutations collected in public databases such as PhyloTree. Experimental results on real and simulated datasets show that our mutation analysis methods作者: obstruct 時(shí)間: 2025-3-29 09:07
https://doi.org/10.1007/978-3-8351-9029-0s challenging as the cells exhibit diverse visual appearance in the crowded cellular image. This task is also less studied by computational methods so far. This paper proposes a . (CRDet) to alleviate the detection difficulties. CRDet is composed of a Cascade RCNN architecture and a dedicated devise作者: acrimony 時(shí)間: 2025-3-29 15:10 作者: Common-Migraine 時(shí)間: 2025-3-29 15:56
https://doi.org/10.1007/978-3-8351-9029-0nomaly (SOPH) syndrome, infantile liver failure syndrome 2 (ILFS2) and a combined severe phenotype including both SOPH and ILFS2 features. Here, we describe a case of a 6-year-old Yakut girl who presented with clinical signs of SOPH syndrome, acute liver failure (ALF) and bone fragility by the type 作者: CLOT 時(shí)間: 2025-3-29 23:15
https://doi.org/10.1007/978-3-322-93111-5he isoform-disease associations helps to uncover the underlying pathology of various complex diseases, and to develop precise treatments and drugs for these diseases. Although many approaches have been proposed for predicting gene-disease associations and isoform functions, few efforts have been mad作者: chronology 時(shí)間: 2025-3-30 01:30 作者: 使熄滅 時(shí)間: 2025-3-30 07:33
Der alte Mensch im Krankenhaus, currently available focus on the classification of reads using a set of reference genomes and their k-mers. While in terms of precision these methods have reached percentages of correctness close to perfection, in terms of recall (the actual number of classified reads) the performances fall at arou作者: 溫和女孩 時(shí)間: 2025-3-30 08:30 作者: TEM 時(shí)間: 2025-3-30 13:23 作者: 怪物 時(shí)間: 2025-3-30 19:20
https://doi.org/10.1007/978-3-662-58792-8, we propose a new approach for mapping long reads to reference genomes. We also propose a new method to generate accurate alignments of the long reads and the corresponding segments of reference genome. The new mapping algorithm is based on the longest common sub-sequence with distance constraints.作者: 使服水土 時(shí)間: 2025-3-30 22:28
Konventionen und Begriffe zu diesem Buch,mors. Compiling a catalog of cancer genes has profound implications for the understanding and treatment of the disease. Existing methods make many implicit and explicit assumptions about the distribution of random mutations. We present FABRIC, a new framework for quantifying the evolutionary selecti作者: Cardioversion 時(shí)間: 2025-3-31 02:18
https://doi.org/10.1007/978-3-642-98096-1is whether there exists a tree ., called an agreement tree, whose taxon set is the union of the taxon sets of the input trees, such that for each ., the restriction of . to the taxon set of . is isomorphic to .. We give a . algorithm for a generalization of the agreement problem in which the input t作者: 冬眠 時(shí)間: 2025-3-31 05:57
Konventionen und Begriffe zu diesem Buch,logies arise to make it possible to find structural variants of as long as ten thousand nucleotides. Thus, long read based structural variant detection has been drawing attention of many recent research projects, and many tools have been developed for long reads to detect structural variants recentl作者: 希望 時(shí)間: 2025-3-31 10:18
Konventionen und Begriffe zu diesem Buch,rgets via traditional biochemical experiments is an extremely laborious, expensive and time-consuming procedure. Therefore, the use of computational methods for predicting potential interactions to guide the experimental verification has attracted a lot of attention. In this paper, we propose a new 作者: 夾克怕包裹 時(shí)間: 2025-3-31 15:57
Konventionen und Begriffe zu diesem Buch,haracterize the pathogenesis of autism spectrum disorder (ASD). Some results have been achieved with machine learning techniques to diagnose ASD with rs-fMRI data. However, most of machine learning methods have neglected the temporal dependency of the time-series fMRI data. In this study, we propose作者: Encapsulate 時(shí)間: 2025-3-31 19:22
Konventionen und Begriffe zu diesem Buch,miRNAs play a key role in many complex human diseases. Therefore, the accurate identification of potential associations between miRNAs and diseases is beneficial to understanding the mechanisms of diseases, developing drugs and treating complex diseases. We propose a new method to predict miRNA-dise作者: Contracture 時(shí)間: 2025-3-31 23:27
Warenbuchungen (ohne Umsatzsteuer),ormation for only a fraction of the taxa. The question is whether this data suffices to construct a reliable phylogeny. The decisiveness problem expresses this question combinatorially. Although a precise characterization of decisiveness is known, the complexity of the problem is open. Here we relat作者: 高歌 時(shí)間: 2025-4-1 03:32
Karlheinz Balzer,Hansotto Pristaffransmission networks is to reconstruct a phylogenetic tree using sequences from disease strains sampled from (a subset of) infected hosts and infer transmissions based on this tree. However, most existing phylogenetic approaches for transmission network inference cannot take within-host strain diver
