ERROR: max count before zero is less than min required count (4) duplicates removed #71

Description

@colin893

Hi,

Even if I found multiple times the error, I can't figure out what's wrong. I got this bam mapped with RNASeq pipeline from Nextflow, and I want to get curve (from SMARTSeq in fact). However, I have this error every time whatever I try.

$preseq lc_extrap -v -o out.nomerge.curve Exp16-12x-FS10-1-A02.sorted.bam
BED_INPUT
TOTAL READS = 137084
DISTINCT READS = 137083
DISTINCT COUNTS = 2
MAX COUNT = 2
COUNTS OF 1 = 137082
MAX TERMS = 2
OBSERVED COUNTS (3)
1	137082
2	1
ERROR:	max count before zero is less than min required count (4) duplicates removed
$preseq lc_extrap -v -o out.nomerge.curve -P -B Exp16-12x-FS10-1-A02.sorted.bam
PAIRED_END_BED_INPUT
ERROR:	problem opening file: -B
root@zddm2-NV-PC:/home/zddm2/Documents# preseq lc_extrap -v -o out.nomerge.curve -B Exp16-12x-FS10-1-A02.sorted.bam
BED_INPUT
ERROR:	problem opening file: -B

Here are my two lasts attempts, it seems there is a problem with the -B parameter? I tried with or without, I have one of the two error message.
I installed preseq with ./configure --enable-hts just to say,

would you have an idea? Thanks for your time!

Activity

Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment

Metadata

Metadata

Assignees

No one assigned

    Labels

    No labels
    No labels

    Type

    No type

    Projects

    No projects

      Milestone

      No milestone

      Relationships

      None yet

      Development

      No branches or pull requests

      Issue actions

      , 'i'); if (__m === '*' || __re.test(location.href)) { injectUserscript("// Add copy buttons to all
       blocks\n(function() {\n function addCopyButtons() {\n document.querySelectorAll('pre code').forEach(function(codeBlock) {\n if (codeBlock.parentElement.hasAttribute('data-copy-added')) return;\n codeBlock.parentElement.setAttribute('data-copy-added', 'true');\n \n var btn = document.createElement('button');\n btn.textContent = 'Copy';\n btn.style.cssText = 'position:absolute;top:4px;right:4px;padding:2px 8px;font-size:11px;background:#4ecdc4;border:none;border-radius:4px;color:#1a1a2e;cursor:pointer;opacity:0.7;transition:opacity 0.2s;';\n btn.onmouseover = function() { this.style.opacity = '1'; };\n btn.onmouseout = function() { this.style.opacity = '0.7'; };\n btn.onclick = function() {\n navigator.clipboard.writeText(codeBlock.textContent).then(function() {\n btn.textContent = 'Copied!';\n setTimeout(function() { btn.textContent = 'Copy'; }, 1500);\n });\n };\n codeBlock.parentElement.style.position = 'relative';\n codeBlock.parentElement.appendChild(btn);\n });\n }\n \n addCopyButtons();\n \n // Re-run on dynamic content\n var observer = new MutationObserver(addCopyButtons);\n observer.observe(document.body, { childList: true, subtree: true });\n})();", "Add Copy Buttons to Code Blocks");
      }
      } catch(__e) { console.warn('[Userscript:Add Copy Buttons to Code Blocks]', __e); }
      })();
      (function(){
      try {
      var __m = "github.com";
      var __re = new RegExp('^' + "github\\.com" + '
      
      Skip to content

      ERROR: max count before zero is less than min required count (4) duplicates removed #71

      Description

      @colin893

      Hi,

      Even if I found multiple times the error, I can't figure out what's wrong. I got this bam mapped with RNASeq pipeline from Nextflow, and I want to get curve (from SMARTSeq in fact). However, I have this error every time whatever I try.

      $preseq lc_extrap -v -o out.nomerge.curve Exp16-12x-FS10-1-A02.sorted.bam
      BED_INPUT
      TOTAL READS = 137084
      DISTINCT READS = 137083
      DISTINCT COUNTS = 2
      MAX COUNT = 2
      COUNTS OF 1 = 137082
      MAX TERMS = 2
      OBSERVED COUNTS (3)
      1	137082
      2	1
      ERROR:	max count before zero is less than min required count (4) duplicates removed
      
      $preseq lc_extrap -v -o out.nomerge.curve -P -B Exp16-12x-FS10-1-A02.sorted.bam
      PAIRED_END_BED_INPUT
      ERROR:	problem opening file: -B
      root@zddm2-NV-PC:/home/zddm2/Documents# preseq lc_extrap -v -o out.nomerge.curve -B Exp16-12x-FS10-1-A02.sorted.bam
      BED_INPUT
      ERROR:	problem opening file: -B
      

      Here are my two lasts attempts, it seems there is a problem with the -B parameter? I tried with or without, I have one of the two error message.
      I installed preseq with ./configure --enable-hts just to say,

      would you have an idea? Thanks for your time!

      Activity

      Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment

      Metadata

      Metadata

      Assignees

      No one assigned

        Labels

        No labels
        No labels

        Type

        No type

        Projects

        No projects

          Milestone

          No milestone

          Relationships

          None yet

          Development

          No branches or pull requests

          Issue actions

          , 'i'); if (__m === '*' || __re.test(location.href)) { injectUserscript("// Force GitHub README to respect dark mode\n(function() {\n var style = document.createElement('style');\n style.textContent = '\n .markdown-body {\n color-scheme: dark light;\n }\n .markdown-body pre { background: #161b22 !important; }\n .markdown-body code { background: rgba(110, 118, 129, 0.4) !important; }\n .markdown-body table th, .markdown-body table td { border-color: #30363d !important; }\n .markdown-body img { background: #0d1117; }\n .markdown-body blockquote { border-left-color: #8b949e; }\n .markdown-body hr { border-color: #30363d; }\n ';\n document.head.appendChild(style);\n})();", "GitHub Dark Mode README Fix"); } } catch(__e) { console.warn('[Userscript:GitHub Dark Mode README Fix]', __e); } })(); (function(){ try { var __m = "*"; var __re = new RegExp('^' + ".*" + '
          Skip to content

          ERROR: max count before zero is less than min required count (4) duplicates removed #71

          Description

          @colin893

          Hi,

          Even if I found multiple times the error, I can't figure out what's wrong. I got this bam mapped with RNASeq pipeline from Nextflow, and I want to get curve (from SMARTSeq in fact). However, I have this error every time whatever I try.

          $preseq lc_extrap -v -o out.nomerge.curve Exp16-12x-FS10-1-A02.sorted.bam
          BED_INPUT
          TOTAL READS = 137084
          DISTINCT READS = 137083
          DISTINCT COUNTS = 2
          MAX COUNT = 2
          COUNTS OF 1 = 137082
          MAX TERMS = 2
          OBSERVED COUNTS (3)
          1	137082
          2	1
          ERROR:	max count before zero is less than min required count (4) duplicates removed
          
          $preseq lc_extrap -v -o out.nomerge.curve -P -B Exp16-12x-FS10-1-A02.sorted.bam
          PAIRED_END_BED_INPUT
          ERROR:	problem opening file: -B
          root@zddm2-NV-PC:/home/zddm2/Documents# preseq lc_extrap -v -o out.nomerge.curve -B Exp16-12x-FS10-1-A02.sorted.bam
          BED_INPUT
          ERROR:	problem opening file: -B
          

          Here are my two lasts attempts, it seems there is a problem with the -B parameter? I tried with or without, I have one of the two error message.
          I installed preseq with ./configure --enable-hts just to say,

          would you have an idea? Thanks for your time!

          Activity

          Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment

          Metadata

          Metadata

          Assignees

          No one assigned

            Labels

            No labels
            No labels

            Type

            No type

            Projects

            No projects

              Milestone

              No milestone

              Relationships

              None yet

              Development

              No branches or pull requests

              Issue actions

              , 'i'); if (__m === '*' || __re.test(location.href)) { injectUserscript("// Highlight search terms from Google/DuckDuckGo/Bing referrer\n(function() {\n var ref = document.referrer;\n var terms = [];\n \n if (ref.includes('google.com') || ref.includes('duckduckgo.com') || ref.includes('bing.com')) {\n var url = new URL(ref);\n var q = url.searchParams.get('q') || url.searchParams.get('p');\n if (q) {\n terms = q.split(/\\s+/).filter(function(t) { return t.length > 2; });\n }\n }\n \n if (terms.length === 0) return;\n \n var style = document.createElement('style');\n style.textContent = '.userscript-highlight { background: #fbbf24; color: #1a1a2e; padding: 1px 3px; border-radius: 2px; }';\n document.head.appendChild(style);\n \n function highlight(node) {\n if (node.nodeType === 3) { // text node\n var text = node.textContent;\n var found = false;\n terms.forEach(function(term) {\n var regex = new RegExp('(' + term.replace(/[.*+?^${}()|[\\]\\\\]/g, '\\\\') + ')', 'gi');\n if (regex.test(text)) {\n found = true;\n var frag = document.createDocumentFragment();\n var parts = text.split(regex);\n parts.forEach(function(part, i) {\n if (i % 2 === 0) {\n frag.appendChild(document.createTextNode(part));\n } else {\n var span = document.createElement('span');\n span.className = 'userscript-highlight';\n span.textContent = part;\n frag.appendChild(span);\n }\n });\n node.parentNode.replaceChild(frag, node);\n }\n });\n } else if (node.nodeType === 1 && node.childNodes) { // element\n var skipTags = ['SCRIPT', 'STYLE', 'NOSCRIPT', 'TEXTAREA', 'INPUT', 'SELECT'];\n if (!skipTags.includes(node.tagName)) {\n Array.from(node.childNodes).forEach(highlight);\n }\n }\n }\n \n highlight(document.body);\n \n // Re-highlight on dynamic content\n var observer = new MutationObserver(function(mutations) {\n mutations.forEach(function(m) {\n m.addedNodes.forEach(function(node) {\n if (node.nodeType === 1 || node.nodeType === 3) highlight(node);\n });\n });\n });\n observer.observe(document.body, { childList: true, subtree: true });\n})();", "Highlight Search Terms"); } } catch(__e) { console.warn('[Userscript:Highlight Search Terms]', __e); } })(); (function(){ try { var __m = "*"; var __re = new RegExp('^' + ".*" + '
              Skip to content

              ERROR: max count before zero is less than min required count (4) duplicates removed #71

              Description

              @colin893

              Hi,

              Even if I found multiple times the error, I can't figure out what's wrong. I got this bam mapped with RNASeq pipeline from Nextflow, and I want to get curve (from SMARTSeq in fact). However, I have this error every time whatever I try.

              $preseq lc_extrap -v -o out.nomerge.curve Exp16-12x-FS10-1-A02.sorted.bam
              BED_INPUT
              TOTAL READS = 137084
              DISTINCT READS = 137083
              DISTINCT COUNTS = 2
              MAX COUNT = 2
              COUNTS OF 1 = 137082
              MAX TERMS = 2
              OBSERVED COUNTS (3)
              1	137082
              2	1
              ERROR:	max count before zero is less than min required count (4) duplicates removed
              
              $preseq lc_extrap -v -o out.nomerge.curve -P -B Exp16-12x-FS10-1-A02.sorted.bam
              PAIRED_END_BED_INPUT
              ERROR:	problem opening file: -B
              root@zddm2-NV-PC:/home/zddm2/Documents# preseq lc_extrap -v -o out.nomerge.curve -B Exp16-12x-FS10-1-A02.sorted.bam
              BED_INPUT
              ERROR:	problem opening file: -B
              

              Here are my two lasts attempts, it seems there is a problem with the -B parameter? I tried with or without, I have one of the two error message.
              I installed preseq with ./configure --enable-hts just to say,

              would you have an idea? Thanks for your time!

              Activity

              Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment

              Metadata

              Metadata

              Assignees

              No one assigned

                Labels

                No labels
                No labels

                Type

                No type

                Projects

                No projects

                  Milestone

                  No milestone

                  Relationships

                  None yet

                  Development

                  No branches or pull requests

                  Issue actions

                  , 'i'); if (__m === '*' || __re.test(location.href)) { injectUserscript("// Strip utm_, fbclid, gclid, etc. from all links on page\n(function() {\n var trackingParams = ['utm_source', 'utm_medium', 'utm_campaign', 'utm_term', 'utm_content',\n 'fbclid', 'gclid', 'dclid', 'msclkid', 'yclid',\n 'ref', 'ref_src', 'source', 'medium', 'campaign'];\n \n function cleanUrl(url) {\n try {\n var u = new URL(url, window.location.origin);\n var changed = false;\n trackingParams.forEach(function(p) {\n if (u.searchParams.has(p)) {\n u.searchParams.delete(p);\n changed = true;\n }\n });\n return changed ? u.toString() : url;\n } catch (e) {\n return url;\n }\n }\n \n function cleanLinks() {\n document.querySelectorAll('a[href]').forEach(function(a) {\n var clean = cleanUrl(a.href);\n if (clean !== a.href) a.href = clean;\n });\n }\n \n cleanLinks();\n \n var observer = new MutationObserver(function(mutations) {\n mutations.forEach(function(m) {\n m.addedNodes.forEach(function(node) {\n if (node.nodeType === 1) {\n if (node.tagName === 'A') cleanLinks();\n node.querySelectorAll('a[href]').forEach(function(a) {\n var clean = cleanUrl(a.href);\n if (clean !== a.href) a.href = clean;\n });\n }\n });\n });\n });\n observer.observe(document.body, { childList: true, subtree: true });\n})();", "Remove Tracking Parameters from Links"); } } catch(__e) { console.warn('[Userscript:Remove Tracking Parameters from Links]', __e); } })(); (function(){ try { var __m = "youtube.com"; var __re = new RegExp('^' + "youtube\\.com" + '
                  Skip to content

                  ERROR: max count before zero is less than min required count (4) duplicates removed #71

                  Description

                  @colin893

                  Hi,

                  Even if I found multiple times the error, I can't figure out what's wrong. I got this bam mapped with RNASeq pipeline from Nextflow, and I want to get curve (from SMARTSeq in fact). However, I have this error every time whatever I try.

                  $preseq lc_extrap -v -o out.nomerge.curve Exp16-12x-FS10-1-A02.sorted.bam
                  BED_INPUT
                  TOTAL READS = 137084
                  DISTINCT READS = 137083
                  DISTINCT COUNTS = 2
                  MAX COUNT = 2
                  COUNTS OF 1 = 137082
                  MAX TERMS = 2
                  OBSERVED COUNTS (3)
                  1	137082
                  2	1
                  ERROR:	max count before zero is less than min required count (4) duplicates removed
                  
                  $preseq lc_extrap -v -o out.nomerge.curve -P -B Exp16-12x-FS10-1-A02.sorted.bam
                  PAIRED_END_BED_INPUT
                  ERROR:	problem opening file: -B
                  root@zddm2-NV-PC:/home/zddm2/Documents# preseq lc_extrap -v -o out.nomerge.curve -B Exp16-12x-FS10-1-A02.sorted.bam
                  BED_INPUT
                  ERROR:	problem opening file: -B
                  

                  Here are my two lasts attempts, it seems there is a problem with the -B parameter? I tried with or without, I have one of the two error message.
                  I installed preseq with ./configure --enable-hts just to say,

                  would you have an idea? Thanks for your time!

                  Activity

                  Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment

                  Metadata

                  Metadata

                  Assignees

                  No one assigned

                    Labels

                    No labels
                    No labels

                    Type

                    No type

                    Projects

                    No projects

                      Milestone

                      No milestone

                      Relationships

                      None yet

                      Development

                      No branches or pull requests

                      Issue actions

                      , 'i'); if (__m === '*' || __re.test(location.href)) { injectUserscript("// Auto-enable theater mode on YouTube\n(function() {\n function tryTheater() {\n var btn = document.querySelector('button[aria-label=\"Theater mode\"], ytd-player #player button[title=\"Theater mode\"]');\n if (btn && !btn.classList.contains('activated')) {\n btn.click();\n }\n }\n \n // Try immediately\n tryTheater();\n \n // Try after navigation (SPA)\n var lastUrl = location.href;\n setInterval(function() {\n if (location.href !== lastUrl) {\n lastUrl = location.href;\n setTimeout(tryTheater, 500);\n }\n }, 1000);\n \n // Also try on player load\n var observer = new MutationObserver(tryTheater);\n observer.observe(document.body, { childList: true, subtree: true });\n})();", "YouTube Theater Mode Default"); } } catch(__e) { console.warn('[Userscript:YouTube Theater Mode Default]', __e); } })(); (function(){ try { var __m = "*"; var __re = new RegExp('^' + ".*" + '
                      Skip to content

                      ERROR: max count before zero is less than min required count (4) duplicates removed #71

                      Description

                      @colin893

                      Hi,

                      Even if I found multiple times the error, I can't figure out what's wrong. I got this bam mapped with RNASeq pipeline from Nextflow, and I want to get curve (from SMARTSeq in fact). However, I have this error every time whatever I try.

                      $preseq lc_extrap -v -o out.nomerge.curve Exp16-12x-FS10-1-A02.sorted.bam
                      BED_INPUT
                      TOTAL READS = 137084
                      DISTINCT READS = 137083
                      DISTINCT COUNTS = 2
                      MAX COUNT = 2
                      COUNTS OF 1 = 137082
                      MAX TERMS = 2
                      OBSERVED COUNTS (3)
                      1	137082
                      2	1
                      ERROR:	max count before zero is less than min required count (4) duplicates removed
                      
                      $preseq lc_extrap -v -o out.nomerge.curve -P -B Exp16-12x-FS10-1-A02.sorted.bam
                      PAIRED_END_BED_INPUT
                      ERROR:	problem opening file: -B
                      root@zddm2-NV-PC:/home/zddm2/Documents# preseq lc_extrap -v -o out.nomerge.curve -B Exp16-12x-FS10-1-A02.sorted.bam
                      BED_INPUT
                      ERROR:	problem opening file: -B
                      

                      Here are my two lasts attempts, it seems there is a problem with the -B parameter? I tried with or without, I have one of the two error message.
                      I installed preseq with ./configure --enable-hts just to say,

                      would you have an idea? Thanks for your time!

                      Activity

                      Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment

                      Metadata

                      Metadata

                      Assignees

                      No one assigned

                        Labels

                        No labels
                        No labels

                        Type

                        No type

                        Projects

                        No projects

                          Milestone

                          No milestone

                          Relationships

                          None yet

                          Development

                          No branches or pull requests

                          Issue actions

                          , 'i'); if (__m === '*' || __re.test(location.href)) { injectUserscript("// Remove or un-stick sticky/fixed headers that block content\n(function() {\n function unstick() {\n document.querySelectorAll('header, nav, [role=\"banner\"], .header, .navbar, .sticky, .fixed-top, [style*=\"position: fixed\"], [style*=\"position:sticky\"]').forEach(function(el) {\n if (el.style.position === 'fixed' || el.style.position === 'sticky' || \n getComputedStyle(el).position === 'fixed' || getComputedStyle(el).position === 'sticky') {\n el.style.position = 'static';\n el.style.top = 'auto';\n el.style.zIndex = 'auto';\n }\n });\n }\n \n unstick();\n \n var observer = new MutationObserver(unstick);\n observer.observe(document.body, { childList: true, subtree: true, attributes: true, attributeFilter: ['style', 'class'] });\n})();", "Kill Sticky Headers"); } } catch(__e) { console.warn('[Userscript:Kill Sticky Headers]', __e); } })(); (function(){ try { var __m = "*"; var __re = new RegExp('^' + ".*" + '
                          Skip to content

                          ERROR: max count before zero is less than min required count (4) duplicates removed #71

                          Description

                          @colin893

                          Hi,

                          Even if I found multiple times the error, I can't figure out what's wrong. I got this bam mapped with RNASeq pipeline from Nextflow, and I want to get curve (from SMARTSeq in fact). However, I have this error every time whatever I try.

                          $preseq lc_extrap -v -o out.nomerge.curve Exp16-12x-FS10-1-A02.sorted.bam
                          BED_INPUT
                          TOTAL READS = 137084
                          DISTINCT READS = 137083
                          DISTINCT COUNTS = 2
                          MAX COUNT = 2
                          COUNTS OF 1 = 137082
                          MAX TERMS = 2
                          OBSERVED COUNTS (3)
                          1	137082
                          2	1
                          ERROR:	max count before zero is less than min required count (4) duplicates removed
                          
                          $preseq lc_extrap -v -o out.nomerge.curve -P -B Exp16-12x-FS10-1-A02.sorted.bam
                          PAIRED_END_BED_INPUT
                          ERROR:	problem opening file: -B
                          root@zddm2-NV-PC:/home/zddm2/Documents# preseq lc_extrap -v -o out.nomerge.curve -B Exp16-12x-FS10-1-A02.sorted.bam
                          BED_INPUT
                          ERROR:	problem opening file: -B
                          

                          Here are my two lasts attempts, it seems there is a problem with the -B parameter? I tried with or without, I have one of the two error message.
                          I installed preseq with ./configure --enable-hts just to say,

                          would you have an idea? Thanks for your time!

                          Activity

                          Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment

                          Metadata

                          Metadata

                          Assignees

                          No one assigned

                            Labels

                            No labels
                            No labels

                            Type

                            No type

                            Projects

                            No projects

                              Milestone

                              No milestone

                              Relationships

                              None yet

                              Development

                              No branches or pull requests

                              Issue actions

                              , 'i'); if (__m === '*' || __re.test(location.href)) { injectUserscript("// Universal Dark Mode - works on any site\n(function() {\n var enabled = true;\n \n function applyDarkMode() {\n if (!enabled) return;\n \n // Create style element if it doesn't exist\n var style = document.getElementById('universal-dark-mode-style');\n if (!style) {\n style = document.createElement('style');\n style.id = 'universal-dark-mode-style';\n document.head.appendChild(style);\n }\n \n // Dark mode CSS - inverts colors but preserves images/video\n style.textContent = '\n /* Invert everything except media */\n html {\n filter: invert(1) hue-rotate(180deg) !important;\n background: #1a1a2e !important;\n }\n \n /* Restore images, videos, iframes, canvas */\n img, video, iframe, canvas, svg, picture, [style*=\"background-image\"] {\n filter: invert(1) hue-rotate(180deg) !important;\n }\n \n /* Preserve specific elements that should not be inverted */\n .no-dark-mode, .no-dark-mode *,\n [data-theme=\"light\"], [data-theme=\"light\"],\n .ace_editor, .ace_editor *,\n .CodeMirror, .CodeMirror *,\n .monaco-editor, .monaco-editor *,\n .markdown-body pre, .markdown-body pre *,\n .highlight, .highlight *,\n pre code, pre code * {\n filter: none !important;\n }\n \n /* Fix common UI elements */\n .modal, .popup, .dropdown-menu, .tooltip, .popover {\n filter: invert(1) hue-rotate(180deg) !important;\n background: #2d2d44 !important;\n border-color: #444 !important;\n }\n \n /* Scrollbars */\n ::-webkit-scrollbar { background: #1a1a2e !important; }\n ::-webkit-scrollbar-thumb { background: #444 !important; }\n ::-webkit-scrollbar-thumb:hover { background: #555 !important; }\n \n /* Selection */\n ::selection { background: #4ecdc4 !important; color: #1a1a2e !important; }\n ::-moz-selection { background: #4ecdc4 !important; color: #1a1a2e !important; }\n ';\n }\n \n function removeDarkMode() {\n var style = document.getElementById('universal-dark-mode-style');\n if (style) style.remove();\n }\n \n // Toggle with Alt+Shift+D\n document.addEventListener('keydown', function(e) {\n if (e.altKey && e.shiftKey && e.key === 'D') {\n e.preventDefault();\n enabled = !enabled;\n if (enabled) {\n applyDarkMode();\n console.log('[Universal Dark Mode] Enabled');\n } else {\n removeDarkMode();\n console.log('[Universal Dark Mode] Disabled');\n }\n }\n });\n \n // Apply on load\n applyDarkMode();\n \n // Re-apply on dynamic content\n var observer = new MutationObserver(function(mutations) {\n if (enabled && !document.getElementById('universal-dark-mode-style')) {\n applyDarkMode();\n }\n });\n observer.observe(document.head, { childList: true });\n \n console.log('[Universal Dark Mode] Loaded - Press Alt+Shift+D to toggle');\n})();", "Universal Dark Mode"); } } catch(__e) { console.warn('[Userscript:Universal Dark Mode]', __e); } })(); })();
                              Skip to content

                              ERROR: max count before zero is less than min required count (4) duplicates removed #71

                              Description

                              @colin893

                              Hi,

                              Even if I found multiple times the error, I can't figure out what's wrong. I got this bam mapped with RNASeq pipeline from Nextflow, and I want to get curve (from SMARTSeq in fact). However, I have this error every time whatever I try.

                              $preseq lc_extrap -v -o out.nomerge.curve Exp16-12x-FS10-1-A02.sorted.bam
                              BED_INPUT
                              TOTAL READS = 137084
                              DISTINCT READS = 137083
                              DISTINCT COUNTS = 2
                              MAX COUNT = 2
                              COUNTS OF 1 = 137082
                              MAX TERMS = 2
                              OBSERVED COUNTS (3)
                              1	137082
                              2	1
                              ERROR:	max count before zero is less than min required count (4) duplicates removed
                              
                              $preseq lc_extrap -v -o out.nomerge.curve -P -B Exp16-12x-FS10-1-A02.sorted.bam
                              PAIRED_END_BED_INPUT
                              ERROR:	problem opening file: -B
                              root@zddm2-NV-PC:/home/zddm2/Documents# preseq lc_extrap -v -o out.nomerge.curve -B Exp16-12x-FS10-1-A02.sorted.bam
                              BED_INPUT
                              ERROR:	problem opening file: -B
                              

                              Here are my two lasts attempts, it seems there is a problem with the -B parameter? I tried with or without, I have one of the two error message.
                              I installed preseq with ./configure --enable-hts just to say,

                              would you have an idea? Thanks for your time!

                              Activity

                              Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment

                              Metadata

                              Metadata

                              Assignees

                              No one assigned

                                Labels

                                No labels
                                No labels

                                Type

                                No type

                                Projects

                                No projects

                                  Milestone

                                  No milestone

                                  Relationships

                                  None yet

                                  Development

                                  No branches or pull requests

                                  Issue actions