Complementing a Strand of DNA

Problem
In DNA strings, symbols 'A' and 'T' are complements of each other, as are 'C' and 'G'.
The reverse complement of a DNA string s is the string sc formed by reversing the symbols of s, then taking the complement of each symbol (e.g., the reverse complement of "GTCA" is "TGAC").
Given: A DNA string s of length at most 1000 bp.
Return: The reverse complement sc of s.
Sample Dataset
AAAACCCGGT
Sample Output

ACCGGGTTTT


#include <stdio.h>
void main ()
{
	char s[9999];
	int i=0;
	int cnt  =0;
	int cnt_a=0;
	int cnt_c=0;
	int cnt_g=0;
	int cnt_t=0;
	puts("输入:\n");
	gets(s);
	for(i=0;s[i]!='\0';i++)
	{
	
		if (s[i] == 'C')
		{
			s[i]  = 'G';
			continue;
		}

		if (s[i] == 'G')
		{
			s[i]  = 'C';
			continue;
		}

		if (s[i] == 'T')
		{
			s[i]  = 'A';
			continue;
		}

		if (s[i] == 'A')
		{
			s[i]  = 'T';
			continue;			
		}

	}
	cnt = i;
	for(;cnt>0;cnt--)
	{
		printf("%c",s[cnt-1]);
	}
}


内容概要:本文提出了一种基于融合鱼鹰算法和柯西变异的改进麻雀优化算法(OCSSA),用于优化变分模态分解(VMD)的参数,进而结合卷积神经网络(CNN)与双向长短期记忆网络(BiLSTM)构建OCSSA-VMD-CNN-BILSTM模型,实现对轴承故障的高【轴承故障诊断】基于融合鱼鹰和柯西变异的麻雀优化算法OCSSA-VMD-CNN-BILSTM轴承诊断研究【西储大学数据】(Matlab代码实现)精度诊断。研究采用西储大学公开的轴承故障数据集进行实验验证,通过优化VMD的模态数和惩罚因子,有效提升了信号分解的准确性与稳定性,随后利用CNN提取故障特征,BiLSTM捕捉时间序列的深层依赖关系,最终实现故障类型的智能识别。该方法在提升故障诊断精度与鲁棒性方面表现出优越性能。; 适合人群:具备一定信号处理、机器学习基础,从事机械故障诊断、智能运维、工业大数据分析等相关领域的研究生、科研人员及工程技术人员。; 使用场景及目标:①解决传统VMD参数依赖人工经验选取的问题,实现参数自适应优化;②提升复杂工况下滚动轴承早期故障的识别准确率;③为智能制造与预测性维护提供可靠的技术支持。; 阅读建议:建议读者结合Matlab代码实现过程,深入理解OCSSA优化机制、VMD信号分解流程以及CNN-BiLSTM网络架构的设计逻辑,重点关注参数优化与故障分类的联动关系,并可通过更换数据集进一步验证模型泛化能力。
Compared with homogeneous network-based methods, het- erogeneous network-based treatment is closer to reality, due to the different kinds of entities with various kinds of relations [22– 24]. In recent years, knowledge graph (KG) has been utilized for data integration and federation [11, 17]. It allows the knowledge graph embedding (KGE) model to excel in the link prediction tasks [18, 19]. For example, Dai et al. provided a method using Wasser- stein adversarial autoencoder-based KGE, which can solve the problem of vanishing gradient on the discrete representation and exploit autoencoder to generate high-quality negative samples [20]. The SumGNN model proposed by Yu et al. succeeds in inte- grating external information of KG by combining high-quality fea- tures and multi-channel knowledge of the sub-graph [21]. Lin et al. proposed KGNN to predict DDI only based on triple facts of KG [66]. Although these methods have used KG information, only focusing on the triple facts or simple data fusion can limit performance and inductive capability [69]. Su et al. successively proposed two DDIs prediction methods [55, 56]. The first one is an end-to-end model called KG2ECapsule based on the biomedical knowledge graph (BKG), which can generate high-quality negative samples and make predictions through feature recursively propagating. Another one learns both drug attributes and triple facts based on attention to extract global representation and obtains good performance. However, these methods also have limited ability or ignore the merging of information from multiple perspectives. Apart from the above, the single perspective has many limitations, such as the need to ensure the integrity of related descriptions, just as network-based methods cannot process new nodes [65]. So, the methods only based on network are not inductive, causing limited generalization [69]. However, it can be alleviated by fully using the intrinsic property of the drug seen as local information, such as chemical structure (CS) [40]. And a handful of existing frameworks can effectively integrate multi-information without losing induction [69]. Thus, there is a necessity for us to propose an effective model to fully learn and fuse the local and global infor- mation for improving performance of DDI identification through multiple information complementing.是什么意思
06-11
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