cy of sample mean X

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国际贸易实务部分

国际贸易实务部分

一、常用的计量单位 1、重量(Weight) 吨(Metric Ton ,M/T ),公斤(Kilogram, Kg ),克( Gram, g),磅(Pound, lb ),盎司(Ounce, oz )等 2、个数 件、个、只(Piece,pc),套(Set),打(Dozen, doz)等 3、长度 米(Meter,m),英尺(Foot,ft),码(Yard,yd)等 4、面积 平方米(Square Meter,sqm)等 5、体积 立方米(Cubic Meter,cum)等 6、容积 升(Liter,l),加仑(Gallon,gal),蒲耳式(Bushel,bu.)
第五节:佣金和折扣
佣金(Commission)
—— 中间商介绍交易或代买代卖而收取的报酬。 在合同或发票中明示的称“明佣”,常用佣金率表示。 例:USD200/Doz. CIF SAN FRANCISCO INCLUDING 5% COMMISSION . 简写为: USD 200/Doz . CIFC5 SAN FRANCISCO 佣金计算公式:佣金=含佣价×佣金率 净价=含佣价-佣金 佣金一般由卖方收到货款后另行支付给中间商。
第三节 其他七种贸易术语
FAS
Free Alongside Ship ( … named port of shipment ) —— 船边交货 ( … 指定装运港) 卖方的义务是在指定的装运港将货物放置于船边时,交货完成,风险转移。 FAS与FOB类似,主要区别在于交货风险转移点,FAS在船边,FOB在船舷。
国际贸易实务部分
Annual Work Summary Report
汇报人 | 小智
第一节 贸易术语概述 一、贸易术语(Trade Terms) —— 是一种表示在国际贸易中,交易双方有关责任、费用与风险划分的专门用语。 二、关于贸易术语的国际贸易惯例 《1932年华沙-牛津规则》 (Warsaw-Oxford Rules) 《1941年美国对外贸易定义修正本》(Revised American Foreign Trade Definitions 1941) 《2000年国际贸易术语解释通则》(INCOTERMS2000) 该通则由国际商会制定,共分为四组13种。

meanshift算法简介

meanshift算法简介

怎样找到数据集合中数据最密集的地方呢?
数据最密集的地方,对应于概率密度最大的地方。我们可 以对概率密度求梯度,梯度的方向就是概率密度增加最大 的方向,从而也就是数据最密集的方向。

,假设除了有限个点,轮廓函数 的梯度对所

均存在 。将 作为轮廓函数,核函数 为:
fh,K
x
2ck ,d n nhd 2 i1
Meanshift算法的概述及其应用
Meanshift的背景
Mean Shift 这个概念最早是由Fukunaga等人于 1975年在一篇关于概率密度梯度函数的估计中提出 来的,其最初含义正如其名,就是偏移的均值向量。
直到20年以后,也就是1995年,,Yizong Cheng发 表了一篇对均值漂移算法里程碑意义的文章。对基 本的Mean Shift算法在以下两个方面做了改进,首先 Yizong Cheng定义了一族核函数,使得随着样本与 被偏移点的距离不同,其偏移量对均值偏移向量的贡 献也不同,其次Yizong Cheng还设定了一个权重系 数,使得不同的样本点重要性不一样,这大大扩大了 Mean Shift的适用范围.另外Yizong Cheng指出了 Mean Shift可能应用的领域,并给出了具体的例子。
• 一维下的无参数估计 设X1,X2, …Xn是从总体中抽出的独立同分布
的样本,X具有未知的密度函数f(x),则f (x)的核估计为:
h为核函数的带宽。常用的核函数如下:
分别是单位均匀核函数 和单位高斯核函数
多维空间下的无参密度估计:
在d维欧式空间X中,x表示该空间中的一个点, 表示该空间中的
核函数,
(5)若
,则停止;否则y0←y1转步骤②。
限制条件:新目标中心需位于原目标中 心附近。

origin菜单栏的中文解释

origin菜单栏的中文解释

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贫血血常规报告英文版

贫血血常规报告英文版

贫血血常规报告英文版Hematology Report for AnemiaPatient Information:Name: [Patient Name]Age: [Patient Age]Gender: [Patient Gender]Date of Report: [Date]Complete Blood Count (CBC) Results:- Hemoglobin: [Value] g/dL (normal range: [Normal Range for Hemoglobin] g/dL)- Hematocrit: [Value] % (normal range: [Normal Range for Hematocrit] %)- Red Blood Cell Count (RBC): [Value] × 10^12/L (normal range: [Normal Range for RBC] × 10^12/L)- Mean Corpuscular Volume (MCV): [Value] fL (normal range: [Normal Range for MCV] fL)- Mean Corpuscular Hemoglobin (MCH): [Value] pg (normal range: [Normal Range for MCH] pg)- Mean Corpuscular Hemoglobin Concentration (MCHC): [Value] g/dL (normal range: [Normal Range for MCHC] g/dL)- Red Cell Distribution Width (RDW): [Value] % (normal range: [Normal Range for RDW] %)Peripheral Blood Smear Findings:- Microcytic hypochromic red blood cells observed.- Anisocytosis and poikilocytosis noted.- Presence of target cells and occasional elliptocytes.- Mild to moderate variation in cell size observed.- Nucleated red blood cells not detected.Interpretation:The hematology report for the patient indicates the presence of microcytic hypochromic anemia. Low hemoglobin and hematocrit levels, as well as reduced red blood cell count (RBC), suggest a possible iron deficiency anemia.The mean corpuscular volume (MCV) is below the normal range, indicating smaller than normal red blood cells. Mean corpuscular hemoglobin (MCH) and mean corpuscular hemoglobin concentration (MCHC) are also reduced, further supporting the diagnosis of hypochromic anemia.The peripheral blood smear findings show microcytic cells with reduced color intensity (hypochromia). Additionally, anisocytosis (variation in cell size) and poikilocytosis (abnormal cell shapes) are present. The presence of target cells and occasional elliptocytes further supports the diagnosis of iron deficiency anemia.The absence of nucleated red blood cells suggests that the anemia is not due to increased destruction or ineffective production of red blood cells.Further investigation is needed to determine the underlying cause of the anemia, such as iron deficiency, chronic disease, or other nutritional deficiencies. Additional tests, medical history review, and possibly consultation with a hematologist or other specialists may be required for a comprehensive diagnosis and appropriate treatment.。

BD FACSCanto

BD FACSCanto

Designing BD™ CBA Flex Set Templates for Flow Cytometers RunningBD FACSDiva™ SoftwareThe following setup procedure is for the BD FACSCanto™, BD™ LSR II, and BD FACSAria™ flow cytometers.1. Prepare 5 tubes labeled: A9, PE-F1, F1, F9, and A1. Vortex the stock vials of beads, add 200 µl of Wash Bufferto each tube followed by 25 µl of the corresponding setup beads.2. Edit the parameters list to display only the following: FSC-A, FSC-W, SSC-A, SSC-W, PE-A, APC-A, andAPC-Cy7-A.3. On a global worksheet, create the following plots: FSC-A/SSC-A dot plot, APC/APC-Cy7 dot plot, and PEhistogram.4. Set FSC-A and SSC-A to Log and create a statistics view showing the FSC-A and SSC-A means. Set the eventsto display to 500. Using the A9 setup beads, adjust FSC and SSC so that the singlet beads have a mean of30,000 for each parameter. Stop acquisition to avoid running out of sample.5. Adjust the FSC-A and SSC-A thresholds using the mean channel as a guideline. Be sure that the thresholdsdo not cut into the bead population.6. In the FSC-A vs SSC-A dot plot, create a region that includes the singlet population of beads. In thePopulation Hierarchy, rename that region singlet.7. Edit the statistics view to display the PE, APC, and APC-Cy7 mean of the singlet beads.8. Through the singlet gate, run the A9 setup beads and adjust the APC and APC-Cy7 voltages until the meanof each parameter is 160,000 ±2,000.9. Through the singlet gate, run the PE-F1 tube and adjust the PE voltage so that the mean is 65 ±5.10. Create compensation controls and delete the PE compensation tube. Run beads as follows for compensationcontrols:Unstained: F1APC Stained: F9APC-Cy7 Stained: A111. Calculate compensation.12. Optional: Verify instrument settings prior to analyzing the assay by recording a sample using the remainingmixed capture beads from the Flex Set assay, export as FCS2.0, and go to Tools > Clustering Test in FCAPArray to see if it can identify the correct number of bead clusters.Set events to record to 300 events per analyte (eg, 300 x 6 = 1800 events for a 6 plex) and set the singlet gate as the storage gate and stopping gate to ensure that only singlet bead events are recorded. Change events to display to 5,000. Record samples and export as FCS2.0 files for analysis in FCAP Array.The Experiment can be saved as a template for future experiments, however it is recommended to verify instrument settings (ie, voltages and compensation) prior to each experiment.Page 1 of 2BD BiosciencesFor country-specific contact information, visit /how_to_orderUnless otherwise specified, all products are for Research Use Only. Not for use in diagnostic or therapeutic procedures. Not for resale.TroubleshootingProblem Possible SolutionBead clusters merging or failure to identify correct number of clusters Check daily QC results for indications of poor laser alignment (increased CV) or PMT sensitivity (decreased MFI at QC instrument settings).Verify that the Window Extension is appropriately set. Approximate values are as follows:BD LSR II: 10BD FACSCanto: 7BD FACSAria: 2Adjust flow rate. Resolution can improve at lower flow rates.Debris (FSC/SSC) during sample acquisition Increase the threshold or enable dual FSC and SSC thresholds. Establish the bead singlet gate asthe storage gate and the stopping gate. Use caution as excluded events cannot be recoveredpost-acquisition.Low event count The beads can precipitate, thoroughly vortex individual capture bead bulk vials prior topreparation of master bead mix and vortex the master bead mix prior to dispensing intothe individual sample tubes. Vortex sample tubes prior to acquisition.Ensure the stopping gate, storage gate, singlet gate, and thresholds are set correctly.Avoid aspiration of beads during wash step.Page 2 of 2BD BiosciencesFor country-specific contact information, visit /how_to_orderUnless otherwise specified, all products are for Research Use Only. Not for use in diagnostic or therapeutic procedures. Not for resale.。

testo 184 USB型 运输数据记录仪 使用手册说明书

testo 184 USB型 运输数据记录仪 使用手册说明书

testo 184 · USB型 运输数据记录仪 使用手册21 内容1内容1内容 (3)2安全与环境 (4)2.1.关于此文档 (4)2.2.确保安全 (4)2.3.保护环境 (4)3说明 (5)3.1.使用 (5)3.2.技术数据 (5)4产品描述 (15)4.1. LED 状况 (15)4.2.显示器(LCD) (16)4.3.按键功能 (17)4.4.重要信息和术语解释 (19)5产品使用 (21)5.1.配置数记录仪 (21)5.2.测量 (23)5.3.读取数据 (24)6产品维护 (26)6.1.更换电池 (26)6.2.清洁仪器 (27)7提示和帮助 (28)32 安全与环境2安全与环境2.1.关于此文档应用>本操作手册是本产品的一个重要组成部分。

>在使用之前仔细通读本文档并熟悉本产品。

要特别注意安全说明和警告,以避免人员受伤和产品损坏。

>请将本文档放在附近,以便在需要时可查阅。

>确保产品的后续用户能够阅读本操作手册。

2.2.确保安全>请正确操作本产品,本产品只能用于指定用途,并且在设定技术数据的参数范围内使用。

请不要强行操作。

>如果外壳损坏,请勿使用本产品。

>只可按照文件中的规定对此设备执行维护和修理工作。

应当严格地遵照规定步聚。

只能使用 Testo 原装备件。

2.3.保护环境>根据合理且合法的规范处理有问题的可充电电池/废弃电池。

>使用寿命到期后,请把本产品送至电子电气装置分类收集处(请遵循当地法律法规),或者返回 Testo 进行处理。

WEEE Reg. Nr. DE 7533435243 说明533.1. 说明使用testo 184 USB 型数据记录仪用于存储和读取单个测量值和测量序列。

它们是专为冷链产品的运输监控而设计。

温度和湿度测量值在整个测量程序持续期间被存储。

加速度测量值在整个测量程序持续期间被监控,并在超过设定的限制值时被存储。

python 散点拟合圆 最小二乘法

python 散点拟合圆 最小二乘法

python 散点拟合圆最小二乘法在Python中,我们可以使用最小二乘法对散点进行拟合,从而找到最佳拟合圆。

首先,我们需要导入一些必要的库,如numpy和scipy:```pythonimport numpy as npfrom scipy.optimize import least_squares```接下来,我们定义一个函数来计算圆心和半径的误差:```pythondef calculate_residuals(params, x, y):# 提取圆心坐标和半径cx, cy, r = params# 计算每个点到圆的距离distances = np.sqrt((x - cx) ** 2 + (y - cy) ** 2) - rreturn distances```然后,我们定义一个函数来拟合散点:```pythondef fit_circle(x, y):# 初始估计值cx_initial = np.mean(x)cy_initial = np.mean(y)r_initial = np.mean(np.sqrt((x - cx_initial) ** 2 + (y - cy_initial) ** 2))# 初始参数params_initial = np.array([cx_initial, cy_initial,r_initial])# 用最小二乘法进行拟合result = least_squares(calculate_residuals,params_initial, args=(x, y))# 提取拟合结果cx_fit, cy_fit, r_fit = result.xreturn cx_fit, cy_fit, r_fit```最后,我们可以使用上面的函数来拟合散点并得到最佳拟合圆:```python# 输入散点坐标x = np.array([1, 2, 3, 4, 5])y = np.array([2, 4, 6, 8, 10])# 拟合散点cx_fit, cy_fit, r_fit = fit_circle(x, y)# 输出最佳拟合圆的圆心和半径print("最佳拟合圆的圆心坐标为 ({}, {}),半径为 {}。

常用中英对照表

常用中英对照表
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• SD(X-Y) = sqrt [ SD(X)2 + SD(Y)2] < SD(X) + SD (Y)
• • Let X1 , X2 be the length of two independent phone calls (the phone call example : mean=2.5 minutes, SD=1 minute) • Let T=X1+X2 • What is the variance of T? (=1+1) SD of T? (=sqrt 2) • Sample size n=4 • T= X1 + X2 + X3+X4 • Var (T) = 1 + 1 + 1 + 1 =4 SD(T)= sqrt 4 =2
Another example: from page 305 of book
• • • • • • Individual 2-SE interval 2-SE interval for the difference Overlapping case Mean X=14, SE =1.2 Mean Y=10, SE=1.1 SE for difference of mean = sqrt (1.22+1.12)=1.627
=Squared root = sqrt
Difference of two sample means
• Assume independence • Example: Does body position for epidural injections affect labor pain? Page 303, textbook, National Women’s Hospital in Auckland : number of spinal segments blocked by the anesthetic • Lying group : n1 =48, mean=8.8, SD=4.4 • Sitting group : n2=35, mean=7.1, SD=4.5 • Question : do we have enough evidence to tell which is better? • SD of difference in mean = .9909, two-standard error interval : [-0.3, 3.7]. Ans. No.
Lecture 7 Accuracy of sample mean X
Var (X)= Var (X) divided by sample size n
What is X bar ? Called sample mean. Standard error of the mean =SD(X) = SD (X) divided by squared root of n As sample size increases, the sample mean become more and more accurate in estimating the population mean • Sample size needed to meet accuracy requirement
Sum of independent random variables from box A, mean µ, SD σ dependent draws X= average of n independent draws
• • • • Var (T) = n σ2 ; SD(T)= sqrt n times σ ; X = T/n SD(X)= SD(T) / n = σ/ sqrt n
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